ReP USP - Resultado da busca

Artigo de periodico
Iris coloboma, blepharophimosis, arachnodactyly, joint contractures: beals syndrome and Van den Ende-Gupta syndrome phenotypic similarities (2009)
Rebelo, Camila Carvalho; Furtado, João Marcello Fortes; Honjo, Rachel Sayuri; Veiga, Kledione Falcão; Ramos, Ester Silveira; Ferraz, Victor Evangelista de Faria; Paula, Jayter Silva de
Source: Clinical Dysmorphology. Unidade: FMRP
Subjects: DOENÇAS DA CÓRNEA, CRIANÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REBELO, Camila Carvalho et al. Iris coloboma, blepharophimosis, arachnodactyly, joint contractures: beals syndrome and Van den Ende-Gupta syndrome phenotypic similarities. Clinical Dysmorphology, v. 18, n. 3, p. 142-144, 2009Tradução . . Disponível em: https://doi.org/10.1097/mcd.0b013e32831368ff. Acesso em: 11 nov. 2024.
APA
Rebelo, C. C., Furtado, J. M. F., Honjo, R. S., Veiga, K. F., Ramos, E. S., Ferraz, V. E. de F., & Paula, J. S. de. (2009). Iris coloboma, blepharophimosis, arachnodactyly, joint contractures: beals syndrome and Van den Ende-Gupta syndrome phenotypic similarities. Clinical Dysmorphology, 18( 3), 142-144. doi:10.1097/mcd.0b013e32831368ff
NLM
Rebelo CC, Furtado JMF, Honjo RS, Veiga KF, Ramos ES, Ferraz VE de F, Paula JS de. Iris coloboma, blepharophimosis, arachnodactyly, joint contractures: beals syndrome and Van den Ende-Gupta syndrome phenotypic similarities [Internet]. Clinical Dysmorphology. 2009 ; 18( 3): 142-144.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1097/mcd.0b013e32831368ff
Vancouver
Rebelo CC, Furtado JMF, Honjo RS, Veiga KF, Ramos ES, Ferraz VE de F, Paula JS de. Iris coloboma, blepharophimosis, arachnodactyly, joint contractures: beals syndrome and Van den Ende-Gupta syndrome phenotypic similarities [Internet]. Clinical Dysmorphology. 2009 ; 18( 3): 142-144.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1097/mcd.0b013e32831368ff
Artigo de periodico
Abnormal methylation at the KvDMRI imprinting control region in clinically normal children conceived by assisted reproductive technologies (2009)
Gomes, M. V.; Huber, J.; Ferriani, Rui Alberto; Amaral Neto, A. M.; Ramos, Ester Silveira
Source: Molecular Human Reproduction. Unidade: FMRP
Subjects: REPRODUÇÃO, CRIANÇAS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, M. V. et al. Abnormal methylation at the KvDMRI imprinting control region in clinically normal children conceived by assisted reproductive technologies. Molecular Human Reproduction, v. 15, n. 8, p. 471-477, 2009Tradução . . Disponível em: https://doi.org/10.1093/molehr/gap038. Acesso em: 11 nov. 2024.
APA
Gomes, M. V., Huber, J., Ferriani, R. A., Amaral Neto, A. M., & Ramos, E. S. (2009). Abnormal methylation at the KvDMRI imprinting control region in clinically normal children conceived by assisted reproductive technologies. Molecular Human Reproduction, 15( 8), 471-477. doi:10.1093/molehr/gap038
NLM
Gomes MV, Huber J, Ferriani RA, Amaral Neto AM, Ramos ES. Abnormal methylation at the KvDMRI imprinting control region in clinically normal children conceived by assisted reproductive technologies [Internet]. Molecular Human Reproduction. 2009 ; 15( 8): 471-477.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1093/molehr/gap038
Vancouver
Gomes MV, Huber J, Ferriani RA, Amaral Neto AM, Ramos ES. Abnormal methylation at the KvDMRI imprinting control region in clinically normal children conceived by assisted reproductive technologies [Internet]. Molecular Human Reproduction. 2009 ; 15( 8): 471-477.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1093/molehr/gap038
Artigo de periodico
eNOS haptolotypes associated with gestational hypertension on preeclampsia (2008)
Sandrim, Valéria C.; Palei, Ana C. T.; Cavalli, Ricardo Carvalho; Araújo, Francielle M.; Ramos, Ester Silveira; Duarte, Geraldo; Tanus-Santos, José Eduardo
Source: Pharmacogenomics. Unidade: FMRP
Subjects: POLIMORFISMO, HIPERTENSÃO NA GRAVIDEZ, PRÉ-ECLÂMPSIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANDRIM, Valéria C. et al. eNOS haptolotypes associated with gestational hypertension on preeclampsia. Pharmacogenomics, v. 9, n. 10, p. 1467-1473, 2008Tradução . . Disponível em: https://doi.org/10.2217/14622416.9.10.1467. Acesso em: 11 nov. 2024.
APA
Sandrim, V. C., Palei, A. C. T., Cavalli, R. C., Araújo, F. M., Ramos, E. S., Duarte, G., & Tanus-Santos, J. E. (2008). eNOS haptolotypes associated with gestational hypertension on preeclampsia. Pharmacogenomics, 9( 10), 1467-1473. doi:10.2217/14622416.9.10.1467
NLM
Sandrim VC, Palei ACT, Cavalli RC, Araújo FM, Ramos ES, Duarte G, Tanus-Santos JE. eNOS haptolotypes associated with gestational hypertension on preeclampsia [Internet]. Pharmacogenomics. 2008 ; 9( 10): 1467-1473.[citado 2024 nov. 11 ] Available from: https://doi.org/10.2217/14622416.9.10.1467
Vancouver
Sandrim VC, Palei ACT, Cavalli RC, Araújo FM, Ramos ES, Duarte G, Tanus-Santos JE. eNOS haptolotypes associated with gestational hypertension on preeclampsia [Internet]. Pharmacogenomics. 2008 ; 9( 10): 1467-1473.[citado 2024 nov. 11 ] Available from: https://doi.org/10.2217/14622416.9.10.1467
Artigo de periodico
IGF2/Mboll polymorphism in gir and nelore cattle (2008)
Silva, Andrea Martins da; Rios, Álvaro Fabrício Lopes; Ramos, Ester Silveira; Cardoso, V. L.; Vercesi Filho, A. E.; Lôbo, Raysildo Barbosa; Freitas, M. A. R.
Source: Developments in Biologicals. Unidade: FMRP
Subjects: POLIMORFISMO, GADO NELORE, GENÉTICA ANIMAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Andrea Martins da et al. IGF2/Mboll polymorphism in gir and nelore cattle. Developments in Biologicals, v. 132, p. 287-291, 2008Tradução . . Acesso em: 11 nov. 2024.
APA
Silva, A. M. da, Rios, Á. F. L., Ramos, E. S., Cardoso, V. L., Vercesi Filho, A. E., Lôbo, R. B., & Freitas, M. A. R. (2008). IGF2/Mboll polymorphism in gir and nelore cattle. Developments in Biologicals, 132, 287-291.
NLM
Silva AM da, Rios ÁFL, Ramos ES, Cardoso VL, Vercesi Filho AE, Lôbo RB, Freitas MAR. IGF2/Mboll polymorphism in gir and nelore cattle. Developments in Biologicals. 2008 ; 132 287-291.[citado 2024 nov. 11 ]
Vancouver
Silva AM da, Rios ÁFL, Ramos ES, Cardoso VL, Vercesi Filho AE, Lôbo RB, Freitas MAR. IGF2/Mboll polymorphism in gir and nelore cattle. Developments in Biologicals. 2008 ; 132 287-291.[citado 2024 nov. 11 ]
Artigo de periodico
Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome (2008)
Araújo, A.; Ramos, Ester Silveira
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Assunto: MAPEAMENTO CROMOSSÔMICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARAÚJO, A. e RAMOS, Ester Silveira. Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome. Brazilian Journal of Medical and Biological Research, v. 41, n. 5, p. 368-372, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2008000500004. Acesso em: 11 nov. 2024.
APA
Araújo, A., & Ramos, E. S. (2008). Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome. Brazilian Journal of Medical and Biological Research, 41( 5), 368-372. doi:10.1590/s0100-879x2008000500004
NLM
Araújo A, Ramos ES. Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 5): 368-372.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1590/s0100-879x2008000500004
Vancouver
Araújo A, Ramos ES. Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 5): 368-372.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1590/s0100-879x2008000500004
Artigo de periodico
Velocardiofacail syndrome with a rare t(2:22) (2007)
Huber, Jair; Rainho, Claudia A.; Gomes, Marcus V.; Santos, Silvio Avelino dos; Ramos, Ester Silveira
Source: Clinical Dysmorphology. Unidade: FMRP
Subjects: ANORMALIDADES MÚLTIPLAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HUBER, Jair et al. Velocardiofacail syndrome with a rare t(2:22). Clinical Dysmorphology, v. 16, n. 3, p. 181-183, 2007Tradução . . Disponível em: https://doi.org/10.1097/mcd.0b013e3280fa81de. Acesso em: 11 nov. 2024.
APA
Huber, J., Rainho, C. A., Gomes, M. V., Santos, S. A. dos, & Ramos, E. S. (2007). Velocardiofacail syndrome with a rare t(2:22). Clinical Dysmorphology, 16( 3), 181-183. doi:10.1097/mcd.0b013e3280fa81de
NLM
Huber J, Rainho CA, Gomes MV, Santos SA dos, Ramos ES. Velocardiofacail syndrome with a rare t(2:22) [Internet]. Clinical Dysmorphology. 2007 ; 16( 3): 181-183.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1097/mcd.0b013e3280fa81de
Vancouver
Huber J, Rainho CA, Gomes MV, Santos SA dos, Ramos ES. Velocardiofacail syndrome with a rare t(2:22) [Internet]. Clinical Dysmorphology. 2007 ; 16( 3): 181-183.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1097/mcd.0b013e3280fa81de
Artigo de periodico
Turner syndrome: counseling prior to oocyte donation (2007)
Ramos, Ester Silveira
Source: São Paulo Medical Journal. Unidade: FMRP
Subjects: CROMOSSOMO Y, ACONSELHAMENTO GENÉTICO, OÓCITOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMOS, Ester Silveira. Turner syndrome: counseling prior to oocyte donation. São Paulo Medical Journal, v. 125, n. 2, p. 112-114, 2007Tradução . . Disponível em: https://doi.org/10.1590/s1516-31802007000200009. Acesso em: 11 nov. 2024.
APA
Ramos, E. S. (2007). Turner syndrome: counseling prior to oocyte donation. São Paulo Medical Journal, 125( 2), 112-114. doi:10.1590/s1516-31802007000200009
NLM
Ramos ES. Turner syndrome: counseling prior to oocyte donation [Internet]. São Paulo Medical Journal. 2007 ; 125( 2): 112-114.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1590/s1516-31802007000200009
Vancouver
Ramos ES. Turner syndrome: counseling prior to oocyte donation [Internet]. São Paulo Medical Journal. 2007 ; 125( 2): 112-114.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1590/s1516-31802007000200009
Artigo de periodico
Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2 (2007)
Sandrin-Garcia, Paula; Abramides, Dagma Venturini Marques; Martelli, Lúcia Regina; Ramos, Ester Silveira; Richieri-Costa, Antonio; Passos, Geraldo Aleixo Silva
Source: Molecular and Cellular Biochemistry. Unidades: FOB, FMRP, HRAC, FORP
Subjects: ANORMALIDADES MÚLTIPLAS, ANORMALIDADES CRANIOFACIAIS, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANDRIN-GARCIA, Paula et al. Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2. Molecular and Cellular Biochemistry, v. 303, n. 1/2, p. 9-17, 2007Tradução . . Disponível em: https://doi.org/10.1007/s11010-007-9450-5. Acesso em: 11 nov. 2024.
APA
Sandrin-Garcia, P., Abramides, D. V. M., Martelli, L. R., Ramos, E. S., Richieri-Costa, A., & Passos, G. A. S. (2007). Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2. Molecular and Cellular Biochemistry, 303( 1/2), 9-17. doi:10.1007/s11010-007-9450-5
NLM
Sandrin-Garcia P, Abramides DVM, Martelli LR, Ramos ES, Richieri-Costa A, Passos GAS. Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2 [Internet]. Molecular and Cellular Biochemistry. 2007 ; 303( 1/2): 9-17.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s11010-007-9450-5
Vancouver
Sandrin-Garcia P, Abramides DVM, Martelli LR, Ramos ES, Richieri-Costa A, Passos GAS. Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2 [Internet]. Molecular and Cellular Biochemistry. 2007 ; 303( 1/2): 9-17.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s11010-007-9450-5
Artigo de periodico
The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma (2006)
Huber, J.; Ramos, Ester Silveira
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: POLIMORFISMO, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HUBER, J. e RAMOS, Ester Silveira. The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma. Brazilian Journal of Medical and Biological Research, v. 39, p. 237-241, 2006Tradução . . Acesso em: 11 nov. 2024.
APA
Huber, J., & Ramos, E. S. (2006). The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma. Brazilian Journal of Medical and Biological Research, 39, 237-241.
NLM
Huber J, Ramos ES. The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma. Brazilian Journal of Medical and Biological Research. 2006 ; 39 237-241.[citado 2024 nov. 11 ]
Vancouver
Huber J, Ramos ES. The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma. Brazilian Journal of Medical and Biological Research. 2006 ; 39 237-241.[citado 2024 nov. 11 ]
Artigo de periodico
Genomic-based nursing care for women with turner syndrome: genomic-based nursing care (2006)
Santos, Milena Jorge Simões Flória Lima ; Ramos, Ester Silveira
Source: Revista Latino-Americana de Enfermagem. Unidades: FMRP, EERP
Subjects: GENÉTICA, DIAGNÓSTICO DE ENFERMAGEM, CUIDADOS DE ENFERMAGEM, ACONSELHAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Milena Jorge Simões Flória Lima e RAMOS, Ester Silveira. Genomic-based nursing care for women with turner syndrome: genomic-based nursing care. Revista Latino-Americana de Enfermagem, v. 14, n. 5, p. 645-650, 2006Tradução . . Disponível em: https://doi.org/10.1590/s0104-11692006000500002. Acesso em: 11 nov. 2024.
APA
Santos, M. J. S. F. L., & Ramos, E. S. (2006). Genomic-based nursing care for women with turner syndrome: genomic-based nursing care. Revista Latino-Americana de Enfermagem, 14( 5), 645-650. doi:10.1590/s0104-11692006000500002
NLM
Santos MJSFL, Ramos ES. Genomic-based nursing care for women with turner syndrome: genomic-based nursing care [Internet]. Revista Latino-Americana de Enfermagem. 2006 ; 14( 5): 645-650.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1590/s0104-11692006000500002
Vancouver
Santos MJSFL, Ramos ES. Genomic-based nursing care for women with turner syndrome: genomic-based nursing care [Internet]. Revista Latino-Americana de Enfermagem. 2006 ; 14( 5): 645-650.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1590/s0104-11692006000500002
Artigo de periodico
Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY (2005)
Scrideli, Carlos Alberto; Baruffi, Marcelo R.; Squire, Jeremy A.; Ramos, Ester Silveira; Karaskowa, Jana; Heck, Benjamin; Tone, Luiz Gonzaga
Source: Leukemia Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, PEDIATRIA, LEUCEMIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SCRIDELI, Carlos Alberto et al. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY. Leukemia Research, v. 29, p. 1465-1467, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.leukres.2005.04.022. Acesso em: 11 nov. 2024.
APA
Scrideli, C. A., Baruffi, M. R., Squire, J. A., Ramos, E. S., Karaskowa, J., Heck, B., & Tone, L. G. (2005). Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY. Leukemia Research, 29, 1465-1467. doi:10.1016/j.leukres.2005.04.022
NLM
Scrideli CA, Baruffi MR, Squire JA, Ramos ES, Karaskowa J, Heck B, Tone LG. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY [Internet]. Leukemia Research. 2005 ; 29 1465-1467.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.leukres.2005.04.022
Vancouver
Scrideli CA, Baruffi MR, Squire JA, Ramos ES, Karaskowa J, Heck B, Tone LG. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY [Internet]. Leukemia Research. 2005 ; 29 1465-1467.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.leukres.2005.04.022
Artigo de periodico
Association between birth weight, body mass index and IGF2/ApaI polymorphism (2005)
Gomes, M. V. M.; Soares, M. R.; Pasqualim-Neto, Amadeu; Marcondes, C. R.; Lôbo, Raysildo Barbosa; Ramos, Ester Silveira
Source: Growth Hormone and IGF Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, M. V. M. et al. Association between birth weight, body mass index and IGF2/ApaI polymorphism. Growth Hormone and IGF Research, v. 15, p. 360-362, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.ghir.2005.06.016. Acesso em: 11 nov. 2024.
APA
Gomes, M. V. M., Soares, M. R., Pasqualim-Neto, A., Marcondes, C. R., Lôbo, R. B., & Ramos, E. S. (2005). Association between birth weight, body mass index and IGF2/ApaI polymorphism. Growth Hormone and IGF Research, 15, 360-362. doi:10.1016/j.ghir.2005.06.016
NLM
Gomes MVM, Soares MR, Pasqualim-Neto A, Marcondes CR, Lôbo RB, Ramos ES. Association between birth weight, body mass index and IGF2/ApaI polymorphism [Internet]. Growth Hormone and IGF Research. 2005 ; 15 360-362.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.ghir.2005.06.016
Vancouver
Gomes MVM, Soares MR, Pasqualim-Neto A, Marcondes CR, Lôbo RB, Ramos ES. Association between birth weight, body mass index and IGF2/ApaI polymorphism [Internet]. Growth Hormone and IGF Research. 2005 ; 15 360-362.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.ghir.2005.06.016
Artigo de periodico
Down syndrome and precocious menopause (2005)
Bartmann, Ana Karina; Araújo, Francielle M.; Iannetta, Odilon; Paneto, João C. C.; Martelli, Lúcia Regina; Ramos, Ester Silveira
Source: Journal of Assisted Reproduction and Genetics. Unidade: FMRP
Subjects: SÍNDROME DE DOWN, MENOPAUSA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARTMANN, Ana Karina et al. Down syndrome and precocious menopause. Journal of Assisted Reproduction and Genetics, v. 22, n. 3, p. 129-131, 2005Tradução . . Disponível em: https://doi.org/10.1007/s10815-005-4878-6. Acesso em: 11 nov. 2024.
APA
Bartmann, A. K., Araújo, F. M., Iannetta, O., Paneto, J. C. C., Martelli, L. R., & Ramos, E. S. (2005). Down syndrome and precocious menopause. Journal of Assisted Reproduction and Genetics, 22( 3), 129-131. doi:10.1007/s10815-005-4878-6
NLM
Bartmann AK, Araújo FM, Iannetta O, Paneto JCC, Martelli LR, Ramos ES. Down syndrome and precocious menopause [Internet]. Journal of Assisted Reproduction and Genetics. 2005 ; 22( 3): 129-131.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s10815-005-4878-6
Vancouver
Bartmann AK, Araújo FM, Iannetta O, Paneto JCC, Martelli LR, Ramos ES. Down syndrome and precocious menopause [Internet]. Journal of Assisted Reproduction and Genetics. 2005 ; 22( 3): 129-131.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s10815-005-4878-6
Artigo de periodico-carta/editorial
TSPY detection in blood, buccal, and urine cells of patients with 45,X karyotype [Carta] (2004)
Bartmann, Ana Karina; Ramos, Ester Silveira; Caetano, Lisandra C.; Rios, Álvaro Fabrício Lopes; Vila, Reginaldo A.
Source: American Journal of Medical Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARTMANN, Ana Karina et al. TSPY detection in blood, buccal, and urine cells of patients with 45,X karyotype [Carta]. American Journal of Medical Genetics. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 11 nov. 2024. , 2004
APA
Bartmann, A. K., Ramos, E. S., Caetano, L. C., Rios, Á. F. L., & Vila, R. A. (2004). TSPY detection in blood, buccal, and urine cells of patients with 45,X karyotype [Carta]. American Journal of Medical Genetics. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Bartmann AK, Ramos ES, Caetano LC, Rios ÁFL, Vila RA. TSPY detection in blood, buccal, and urine cells of patients with 45,X karyotype [Carta]. American Journal of Medical Genetics. 2004 ; 130A 320-321.[citado 2024 nov. 11 ]
Vancouver
Bartmann AK, Ramos ES, Caetano LC, Rios ÁFL, Vila RA. TSPY detection in blood, buccal, and urine cells of patients with 45,X karyotype [Carta]. American Journal of Medical Genetics. 2004 ; 130A 320-321.[citado 2024 nov. 11 ]
Artigo de periodico-carta/editorial
Blepharo-Cheilo-Dontic (BCD) syndrome with agenesis of thyroid broadens the phenotype and extends the discussion about the genes [Carta] (2004)
Martinhago, Ciro Dresch; Ramos, Ester Silveira
Source: American Journal of Medical Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARTINHAGO, Ciro Dresch e RAMOS, Ester Silveira. Blepharo-Cheilo-Dontic (BCD) syndrome with agenesis of thyroid broadens the phenotype and extends the discussion about the genes [Carta]. American Journal of Medical Genetics. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 11 nov. 2024. , 2004
APA
Martinhago, C. D., & Ramos, E. S. (2004). Blepharo-Cheilo-Dontic (BCD) syndrome with agenesis of thyroid broadens the phenotype and extends the discussion about the genes [Carta]. American Journal of Medical Genetics. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Martinhago CD, Ramos ES. Blepharo-Cheilo-Dontic (BCD) syndrome with agenesis of thyroid broadens the phenotype and extends the discussion about the genes [Carta]. American Journal of Medical Genetics. 2004 ; 130A 437-438.[citado 2024 nov. 11 ]
Vancouver
Martinhago CD, Ramos ES. Blepharo-Cheilo-Dontic (BCD) syndrome with agenesis of thyroid broadens the phenotype and extends the discussion about the genes [Carta]. American Journal of Medical Genetics. 2004 ; 130A 437-438.[citado 2024 nov. 11 ]
Artigo de periodico
Why do older women have poor implantation rates?: a possible role of the mitochondria (2004)
Bartmann, Ana Karina; Romão, Gustavo Salata; Ramos, Ester Silveira; Ferriani, Rui Alberto
Source: Journal of Assisted Reproduction and Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARTMANN, Ana Karina et al. Why do older women have poor implantation rates?: a possible role of the mitochondria. Journal of Assisted Reproduction and Genetics, v. 21, n. 3, p. 79-83, 2004Tradução . . Acesso em: 11 nov. 2024.
APA
Bartmann, A. K., Romão, G. S., Ramos, E. S., & Ferriani, R. A. (2004). Why do older women have poor implantation rates?: a possible role of the mitochondria. Journal of Assisted Reproduction and Genetics, 21( 3), 79-83.
NLM
Bartmann AK, Romão GS, Ramos ES, Ferriani RA. Why do older women have poor implantation rates?: a possible role of the mitochondria. Journal of Assisted Reproduction and Genetics. 2004 ; 21( 3): 79-83.[citado 2024 nov. 11 ]
Vancouver
Bartmann AK, Romão GS, Ramos ES, Ferriani RA. Why do older women have poor implantation rates?: a possible role of the mitochondria. Journal of Assisted Reproduction and Genetics. 2004 ; 21( 3): 79-83.[citado 2024 nov. 11 ]
Artigo de periodico
Fuhrmann syndrome: two Brazilian cases (2003)
Huber, Jair; Volpon, José Batista; Ramos, Ester Silveira
Source: Clinical Dysmorphology. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HUBER, Jair e VOLPON, José Batista e RAMOS, Ester Silveira. Fuhrmann syndrome: two Brazilian cases. Clinical Dysmorphology, v. 12, n. 2, p. 85-88, 2003Tradução . . Disponível em: https://doi.org/10.1097/00019605-200304000-00002. Acesso em: 11 nov. 2024.
APA
Huber, J., Volpon, J. B., & Ramos, E. S. (2003). Fuhrmann syndrome: two Brazilian cases. Clinical Dysmorphology, 12( 2), 85-88. doi:10.1097/00019605-200304000-00002
NLM
Huber J, Volpon JB, Ramos ES. Fuhrmann syndrome: two Brazilian cases [Internet]. Clinical Dysmorphology. 2003 ; 12( 2): 85-88.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1097/00019605-200304000-00002
Vancouver
Huber J, Volpon JB, Ramos ES. Fuhrmann syndrome: two Brazilian cases [Internet]. Clinical Dysmorphology. 2003 ; 12( 2): 85-88.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1097/00019605-200304000-00002
Artigo de periodico
Noonan syndrome associated with unilateral iris coloboma and congenital chylothorax in an infant (2003)
Carvalho, D. R.; Alves, V. V. B.; Minaré-Júnior, A.; Peres, Luiz César; Pina Neto, João Monteiro de; Ramos, Ester Silveira
Source: Clinical Dysmorphology. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, D. R. et al. Noonan syndrome associated with unilateral iris coloboma and congenital chylothorax in an infant. Clinical Dysmorphology, v. 12, n. 2, p. 143-144, 2003Tradução . . Disponível em: https://doi.org/10.1097/00019605-200304000-00015. Acesso em: 11 nov. 2024.
APA
Carvalho, D. R., Alves, V. V. B., Minaré-Júnior, A., Peres, L. C., Pina Neto, J. M. de, & Ramos, E. S. (2003). Noonan syndrome associated with unilateral iris coloboma and congenital chylothorax in an infant. Clinical Dysmorphology, 12( 2), 143-144. doi:10.1097/00019605-200304000-00015
NLM
Carvalho DR, Alves VVB, Minaré-Júnior A, Peres LC, Pina Neto JM de, Ramos ES. Noonan syndrome associated with unilateral iris coloboma and congenital chylothorax in an infant [Internet]. Clinical Dysmorphology. 2003 ; 12( 2): 143-144.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1097/00019605-200304000-00015
Vancouver
Carvalho DR, Alves VVB, Minaré-Júnior A, Peres LC, Pina Neto JM de, Ramos ES. Noonan syndrome associated with unilateral iris coloboma and congenital chylothorax in an infant [Internet]. Clinical Dysmorphology. 2003 ; 12( 2): 143-144.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1097/00019605-200304000-00015
Artigo de periodico
Beckwith-Wiedemann syndrome and isolated hemihyperplasia (2003)
Gomes, Marcus Vinícius de Matos; Ramos, Ester Silveira
Source: São Paulo Medical Journal. Unidade: FMRP
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, Marcus Vinícius de Matos e RAMOS, Ester Silveira. Beckwith-Wiedemann syndrome and isolated hemihyperplasia. São Paulo Medical Journal, v. 121, n. 3, p. 133-138, 2003Tradução . . Disponível em: https://doi.org/10.1590/s1516-31802003000300010. Acesso em: 11 nov. 2024.
APA
Gomes, M. V. de M., & Ramos, E. S. (2003). Beckwith-Wiedemann syndrome and isolated hemihyperplasia. São Paulo Medical Journal, 121( 3), 133-138. doi:10.1590/s1516-31802003000300010
NLM
Gomes MV de M, Ramos ES. Beckwith-Wiedemann syndrome and isolated hemihyperplasia [Internet]. São Paulo Medical Journal. 2003 ; 121( 3): 133-138.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1590/s1516-31802003000300010
Vancouver
Gomes MV de M, Ramos ES. Beckwith-Wiedemann syndrome and isolated hemihyperplasia [Internet]. São Paulo Medical Journal. 2003 ; 121( 3): 133-138.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1590/s1516-31802003000300010
Artigo de periodico
Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome (2002)
Sandrin Garcia, P; Macedo, C; Martelli, Lúcia Regina; Ramos, Ester Silveira; Guion Almeida, Maria Leine; Richieri Costa, Antônio; Passos, Geraldo Aleixo Silva
Source: Clinical genetics. Unidades: FMRP, HRAC, FORP
Subjects: GENÉTICA, DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANDRIN GARCIA, P et al. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome. Clinical genetics, v. 61, n. 5, p. 380-383, 2002Tradução . . Disponível em: https://doi.org/10.1034/j.1399-0004.2002.610511.x. Acesso em: 11 nov. 2024.
APA
Sandrin Garcia, P., Macedo, C., Martelli, L. R., Ramos, E. S., Guion Almeida, M. L., Richieri Costa, A., & Passos, G. A. S. (2002). Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome. Clinical genetics, 61( 5), 380-383. doi:10.1034/j.1399-0004.2002.610511.x
NLM
Sandrin Garcia P, Macedo C, Martelli LR, Ramos ES, Guion Almeida ML, Richieri Costa A, Passos GAS. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome [Internet]. Clinical genetics. 2002 ; 61( 5): 380-383.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1034/j.1399-0004.2002.610511.x
Vancouver
Sandrin Garcia P, Macedo C, Martelli LR, Ramos ES, Guion Almeida ML, Richieri Costa A, Passos GAS. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome [Internet]. Clinical genetics. 2002 ; 61( 5): 380-383.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1034/j.1399-0004.2002.610511.x

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