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Artigo de periodico
Zimmermann-laband syndrome (a new case) (1988)
Pina Neto, J M; Freitas, A C; Ribas, José Paulo
Source: American Journal of Medical Genetics. Unidades: FORP, FMRP
Assunto: MEDICINA
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ABNT
PINA NETO, J M e FREITAS, A C e RIBAS, José Paulo. Zimmermann-laband syndrome (a new case). American Journal of Medical Genetics, v. 87, n. 482, p. 21-4, 1988Tradução . . Acesso em: 19 abr. 2024.
APA
Pina Neto, J. M., Freitas, A. C., & Ribas, J. P. (1988). Zimmermann-laband syndrome (a new case). American Journal of Medical Genetics, 87( 482), 21-4.
NLM
Pina Neto JM, Freitas AC, Ribas JP. Zimmermann-laband syndrome (a new case). American Journal of Medical Genetics. 1988 ;87( 482): 21-4.[citado 2024 abr. 19 ]
Vancouver
Pina Neto JM, Freitas AC, Ribas JP. Zimmermann-laband syndrome (a new case). American Journal of Medical Genetics. 1988 ;87( 482): 21-4.[citado 2024 abr. 19 ]
Artigo de periodico
X-linked syndrome: mental retardation, hip luxation, and g6pd variant ['GD'(+)butantan] (1991)
Stocco dos Santos, R. C.; Barretto, Orlando César de Oliveira; Nonoyama, K.; Castro, N. H. C.; Ferraz, O. P.; Walter Moura, J.; Vescio, C. C. S.; Becak, W.
Source: American Journal of Medical Genetics. Unidade: FM
Assunto: GENÉTICA MÉDICA
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ABNT
STOCCO DOS SANTOS, R. C. et al. X-linked syndrome: mental retardation, hip luxation, and g6pd variant ['GD'(+)butantan]. American Journal of Medical Genetics, v. 39, n. 2, p. 133-136, 1991Tradução . . Acesso em: 19 abr. 2024.
APA
Stocco dos Santos, R. C., Barretto, O. C. de O., Nonoyama, K., Castro, N. H. C., Ferraz, O. P., Walter Moura, J., et al. (1991). X-linked syndrome: mental retardation, hip luxation, and g6pd variant ['GD'(+)butantan]. American Journal of Medical Genetics, 39( 2), 133-136.
NLM
Stocco dos Santos RC, Barretto OC de O, Nonoyama K, Castro NHC, Ferraz OP, Walter Moura J, Vescio CCS, Becak W. X-linked syndrome: mental retardation, hip luxation, and g6pd variant ['GD'(+)butantan]. American Journal of Medical Genetics. 1991 ; 39( 2): 133-136.[citado 2024 abr. 19 ]
Vancouver
Stocco dos Santos RC, Barretto OC de O, Nonoyama K, Castro NHC, Ferraz OP, Walter Moura J, Vescio CCS, Becak W. X-linked syndrome: mental retardation, hip luxation, and g6pd variant ['GD'(+)butantan]. American Journal of Medical Genetics. 1991 ; 39( 2): 133-136.[citado 2024 abr. 19 ]
Artigo de periodico
Waardenburg syndrome: clinical differentiation between types I and II (2003)
Pardono, Eliete; Bever, Yolande van; Ende, Jenneke van den; Havrenne, Poti Chimetta; Iughetti, Paula; Maestrelli, Sylvia Regina Pedrosa; Costa Filho, Orozimbo Alves; Richieri-Costa, Antonio; Frota-Pessoa, Oswaldo; Otto, Paulo A
Source: American Journal of Medical Genetics. Unidades: FOB, HRAC, IB
Assunto: ANORMALIDADES CRANIOFACIAIS
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ABNT
PARDONO, Eliete et al. Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, v. 117A, n. 3, p. 223-235, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10193. Acesso em: 19 abr. 2024.
APA
Pardono, E., Bever, Y. van, Ende, J. van den, Havrenne, P. C., Iughetti, P., Maestrelli, S. R. P., et al. (2003). Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, 117A( 3), 223-235. doi:10.1002/ajmg.a.10193
NLM
Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.10193
Vancouver
Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.10193
Artigo de periodico
Variable expressivity of the acheiropodia gene (1983)
Grimaldi, Angela; Masiero, D; Richieri-Costa, Antonio; Maia, A. Freire
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: ANORMALIDADES CONGÊNITAS, GENES, FENÓTIPOS
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ABNT
GRIMALDI, Angela et al. Variable expressivity of the acheiropodia gene. American Journal of Medical Genetics, v. 16, n. 4, p. 631-634, 1983Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320160420. Acesso em: 19 abr. 2024.
APA
Grimaldi, A., Masiero, D., Richieri-Costa, A., & Maia, A. F. (1983). Variable expressivity of the acheiropodia gene. American Journal of Medical Genetics, 16( 4), 631-634. doi:10.1002/ajmg.1320160420
NLM
Grimaldi A, Masiero D, Richieri-Costa A, Maia AF. Variable expressivity of the acheiropodia gene [Internet]. American Journal of Medical Genetics. 1983 ; 16( 4): 631-634.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320160420
Vancouver
Grimaldi A, Masiero D, Richieri-Costa A, Maia AF. Variable expressivity of the acheiropodia gene [Internet]. American Journal of Medical Genetics. 1983 ; 16( 4): 631-634.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320160420
Artigo de periodico
Urinary tract involvement in EEC syndrome: a clinical study in 25 Brazilian patients (1992)
Nardi, Aguinaldo César ; Ferreira, Ubirajara; Rodrigues Netto, Nelson; Magna, Luís Alberto; Rodini, Elaine Sbroggio de Oliveira; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: SISTEMA URINARIO (FISIOLOGIA)
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ABNT
NARDI, Aguinaldo César et al. Urinary tract involvement in EEC syndrome: a clinical study in 25 Brazilian patients. American Journal of Medical Genetics, v. 44, n. 6, p. 803-806, 1992Tradução . . Acesso em: 19 abr. 2024.
APA
Nardi, A. C., Ferreira, U., Rodrigues Netto, N., Magna, L. A., Rodini, E. S. de O., & Richieri-Costa, A. (1992). Urinary tract involvement in EEC syndrome: a clinical study in 25 Brazilian patients. American Journal of Medical Genetics, 44( 6), 803-806.
NLM
Nardi AC, Ferreira U, Rodrigues Netto N, Magna LA, Rodini ES de O, Richieri-Costa A. Urinary tract involvement in EEC syndrome: a clinical study in 25 Brazilian patients. American Journal of Medical Genetics. 1992 ; 44( 6): 803-806.[citado 2024 abr. 19 ]
Vancouver
Nardi AC, Ferreira U, Rodrigues Netto N, Magna LA, Rodini ES de O, Richieri-Costa A. Urinary tract involvement in EEC syndrome: a clinical study in 25 Brazilian patients. American Journal of Medical Genetics. 1992 ; 44( 6): 803-806.[citado 2024 abr. 19 ]
Artigo de periodico
Unusual type of brachydactyly associated with short stature and facial anomalies: a new syndrome? [Brief clinical report] (1985)
Richieri-Costa, Antonio; Coletto, G M D D; Otto, Paulo A
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA
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ABNT
RICHIERI-COSTA, Antonio e COLETTO, G M D D e OTTO, Paulo A. Unusual type of brachydactyly associated with short stature and facial anomalies: a new syndrome? [Brief clinical report]. American Journal of Medical Genetics, v. 21, n. 4, p. 637-642, 1985Tradução . . Acesso em: 19 abr. 2024.
APA
Richieri-Costa, A., Coletto, G. M. D. D., & Otto, P. A. (1985). Unusual type of brachydactyly associated with short stature and facial anomalies: a new syndrome? [Brief clinical report]. American Journal of Medical Genetics, 21( 4), 637-642.
NLM
Richieri-Costa A, Coletto GMDD, Otto PA. Unusual type of brachydactyly associated with short stature and facial anomalies: a new syndrome? [Brief clinical report]. American Journal of Medical Genetics. 1985 ; 21( 4): 637-642.[citado 2024 abr. 19 ]
Vancouver
Richieri-Costa A, Coletto GMDD, Otto PA. Unusual type of brachydactyly associated with short stature and facial anomalies: a new syndrome? [Brief clinical report]. American Journal of Medical Genetics. 1985 ; 21( 4): 637-642.[citado 2024 abr. 19 ]
Artigo de periodico
Unusual nasal duplication in two patients (2004)
Guion-Almeida, Maria Leine; Lamônica Neto, Domingos; Lopes, Vera Lúcia Gil da Silva
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: NARIZ (ANATOMIA), TOMOGRAFIA COMPUTADORIZADA POR RAIOS X, FENÓTIPOS
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ABNT
GUION-ALMEIDA, Maria Leine e LAMÔNICA NETO, Domingos e LOPES, Vera Lúcia Gil da Silva. Unusual nasal duplication in two patients. American Journal of Medical Genetics, v. No 2004, n. 4, p. 435-436, 2004Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30278. Acesso em: 19 abr. 2024.
APA
Guion-Almeida, M. L., Lamônica Neto, D., & Lopes, V. L. G. da S. (2004). Unusual nasal duplication in two patients. American Journal of Medical Genetics, No 2004( 4), 435-436. doi:10.1002/ajmg.a.30278
NLM
Guion-Almeida ML, Lamônica Neto D, Lopes VLG da S. Unusual nasal duplication in two patients [Internet]. American Journal of Medical Genetics. 2004 ; No 2004( 4): 435-436.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.30278
Vancouver
Guion-Almeida ML, Lamônica Neto D, Lopes VLG da S. Unusual nasal duplication in two patients [Internet]. American Journal of Medical Genetics. 2004 ; No 2004( 4): 435-436.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.30278
Artigo de periodico
Two new brazilian patients with Gómez-López-Hernández syndrome: reviewing the expanded phenotype with molecular insights (2008)
Gomy, Israel; Heck, Benjamin; Santos, Antonio Carlos dos; Figueiredo, Maria Silvia L.; Martinelli Júnior, Carlos Eduardo; Nogueira, Maria Priscila C.; Pina-Neto, João Monteiro
Source: American Journal of Medical Genetics. Unidade: FMRP
Subjects: DOENÇAS DO SISTEMA NERVOSO CENTRAL, MANIFESTAÇÕES NEUROLÓGICAS
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ABNT
GOMY, Israel et al. Two new brazilian patients with Gómez-López-Hernández syndrome: reviewing the expanded phenotype with molecular insights. American Journal of Medical Genetics, v. 146A, p. 649-657, 2008Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32173. Acesso em: 19 abr. 2024.
APA
Gomy, I., Heck, B., Santos, A. C. dos, Figueiredo, M. S. L., Martinelli Júnior, C. E., Nogueira, M. P. C., & Pina-Neto, J. M. (2008). Two new brazilian patients with Gómez-López-Hernández syndrome: reviewing the expanded phenotype with molecular insights. American Journal of Medical Genetics, 146A, 649-657. doi:10.1002/ajmg.a.32173
NLM
Gomy I, Heck B, Santos AC dos, Figueiredo MSL, Martinelli Júnior CE, Nogueira MPC, Pina-Neto JM. Two new brazilian patients with Gómez-López-Hernández syndrome: reviewing the expanded phenotype with molecular insights [Internet]. American Journal of Medical Genetics. 2008 ; 146A 649-657.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.32173
Vancouver
Gomy I, Heck B, Santos AC dos, Figueiredo MSL, Martinelli Júnior CE, Nogueira MPC, Pina-Neto JM. Two new brazilian patients with Gómez-López-Hernández syndrome: reviewing the expanded phenotype with molecular insights [Internet]. American Journal of Medical Genetics. 2008 ; 146A 649-657.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.32173
Artigo de periodico-carta/editorial
Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial] (1999)
Vianna-Morgante, Angela M
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
VIANNA-MORGANTE, Angela M. Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 abr. 2024. , 1999
APA
Vianna-Morgante, A. M. (1999). Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Vianna-Morgante AM. Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial]. American Journal of Medical Genetics. 1999 ; 83( 4): 326.[citado 2024 abr. 19 ]
Vancouver
Vianna-Morgante AM. Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial]. American Journal of Medical Genetics. 1999 ; 83( 4): 326.[citado 2024 abr. 19 ]
Artigo de periodico
Treatment of duchenne muscular dystrophy with growth hormone inhibitors (1986)
Zatz, Mayana ; Betti, R T B; Frota-Pessoa, O
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR (TRATAMENTO), DOENÇAS GENÉTICAS, GENÉTICA, HORMÔNIOS
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ABNT
ZATZ, Mayana e BETTI, R T B e FROTA-PESSOA, O. Treatment of duchenne muscular dystrophy with growth hormone inhibitors. American Journal of Medical Genetics, v. 24, p. 549-66, 1986Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320240322. Acesso em: 19 abr. 2024.
APA
Zatz, M., Betti, R. T. B., & Frota-Pessoa, O. (1986). Treatment of duchenne muscular dystrophy with growth hormone inhibitors. American Journal of Medical Genetics, 24, 549-66. doi:10.1002/ajmg.1320240322
NLM
Zatz M, Betti RTB, Frota-Pessoa O. Treatment of duchenne muscular dystrophy with growth hormone inhibitors [Internet]. American Journal of Medical Genetics. 1986 ;24 549-66.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320240322
Vancouver
Zatz M, Betti RTB, Frota-Pessoa O. Treatment of duchenne muscular dystrophy with growth hormone inhibitors [Internet]. American Journal of Medical Genetics. 1986 ;24 549-66.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320240322
Artigo de periodico-carta/editorial
Transposon-like element in the dystrophin gene. [Carta ao editor] (1993)
Zatz, Mayana ; Passos-Bueno, Maria Rita ; Vainzof, Mariz
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: DISTROFIA MUSCULAR
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ABNT
ZATZ, Mayana e PASSOS-BUENO, Maria Rita e VAINZOF, Mariz. Transposon-like element in the dystrophin gene. [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 abr. 2024. , 1993
APA
Zatz, M., Passos-Bueno, M. R., & Vainzof, M. (1993). Transposon-like element in the dystrophin gene. [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Passos-Bueno MR, Vainzof M. Transposon-like element in the dystrophin gene. [Carta ao editor]. American Journal of Medical Genetics. 1993 ; 46( 5): 601.[citado 2024 abr. 19 ]
Vancouver
Zatz M, Passos-Bueno MR, Vainzof M. Transposon-like element in the dystrophin gene. [Carta ao editor]. American Journal of Medical Genetics. 1993 ; 46( 5): 601.[citado 2024 abr. 19 ]
Artigo de periodico
Tibial hemimelia: report on 37 new cases, clinical and gentic considerations (1987)
Richieri-Costa, A; Ferrareto, I; Masiero, D; Silva, C R M
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, FENÓTIPOS, GENÉTICA MÉDICA
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ABNT
RICHIERI-COSTA, A et al. Tibial hemimelia: report on 37 new cases, clinical and gentic considerations. American Journal of Medical Genetics, v. 27, n. 4 , p. 867-84, 1987Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320270414. Acesso em: 19 abr. 2024.
APA
Richieri-Costa, A., Ferrareto, I., Masiero, D., & Silva, C. R. M. (1987). Tibial hemimelia: report on 37 new cases, clinical and gentic considerations. American Journal of Medical Genetics, 27( 4 ), 867-84. doi:10.1002/ajmg.1320270414
NLM
Richieri-Costa A, Ferrareto I, Masiero D, Silva CRM. Tibial hemimelia: report on 37 new cases, clinical and gentic considerations [Internet]. American Journal of Medical Genetics. 1987 ;27( 4 ): 867-84.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320270414
Vancouver
Richieri-Costa A, Ferrareto I, Masiero D, Silva CRM. Tibial hemimelia: report on 37 new cases, clinical and gentic considerations [Internet]. American Journal of Medical Genetics. 1987 ;27( 4 ): 867-84.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320270414
Artigo de periodico
Tibial hemimelia-cleft lip/palate in a Brazilian child born to consaguineous parents (1987)
Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, FISSURA LÁBIOPALATINA, GENES RECESSIVOS
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ABNT
RICHIERI-COSTA, Antonio. Tibial hemimelia-cleft lip/palate in a Brazilian child born to consaguineous parents. American Journal of Medical Genetics, v. 28, n. 2, p. 325-329, 1987Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320280209. Acesso em: 19 abr. 2024.
APA
Richieri-Costa, A. (1987). Tibial hemimelia-cleft lip/palate in a Brazilian child born to consaguineous parents. American Journal of Medical Genetics, 28( 2), 325-329. doi:10.1002/ajmg.1320280209
NLM
Richieri-Costa A. Tibial hemimelia-cleft lip/palate in a Brazilian child born to consaguineous parents [Internet]. American Journal of Medical Genetics. 1987 ;28( 2): 325-329.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320280209
Vancouver
Richieri-Costa A. Tibial hemimelia-cleft lip/palate in a Brazilian child born to consaguineous parents [Internet]. American Journal of Medical Genetics. 1987 ;28( 2): 325-329.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320280209
Artigo de periodico
Tibial aplasia-ectrodactyly as variant expression of the gollop-wolfgang complex: report of a Brazilian family (1987)
Richieri-Costa, Antonio; Brunoni, Décio; Laredo Filho, José; Kasinski, Silvana
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: GENES RECESSIVOS, REGULAÇÃO GÊNICA, MALFORMAÇÕES
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ABNT
RICHIERI-COSTA, Antonio et al. Tibial aplasia-ectrodactyly as variant expression of the gollop-wolfgang complex: report of a Brazilian family. American Journal of Medical Genetics, v. 28, n. 4, p. 971-980, 1987Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320280424. Acesso em: 19 abr. 2024.
APA
Richieri-Costa, A., Brunoni, D., Laredo Filho, J., & Kasinski, S. (1987). Tibial aplasia-ectrodactyly as variant expression of the gollop-wolfgang complex: report of a Brazilian family. American Journal of Medical Genetics, 28( 4), 971-980. doi:10.1002/ajmg.1320280424
NLM
Richieri-Costa A, Brunoni D, Laredo Filho J, Kasinski S. Tibial aplasia-ectrodactyly as variant expression of the gollop-wolfgang complex: report of a Brazilian family [Internet]. American Journal of Medical Genetics. 1987 ; 28( 4): 971-980.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320280424
Vancouver
Richieri-Costa A, Brunoni D, Laredo Filho J, Kasinski S. Tibial aplasia-ectrodactyly as variant expression of the gollop-wolfgang complex: report of a Brazilian family [Internet]. American Journal of Medical Genetics. 1987 ; 28( 4): 971-980.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320280424
Artigo de periodico
Three new cases of spondylocarpotarsal synostosis syndrome: clinical and radiographic studies (1998)
Coêlho, Kátia-Édni F A; Ramos, Ester Silveira; Félix, Têmis Maria; Martelli, Lucia Regina; Pina Neto, João Monteiro de; Niikawa, Norio
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
COÊLHO, Kátia-Édni F A et al. Three new cases of spondylocarpotarsal synostosis syndrome: clinical and radiographic studies. American Journal of Medical Genetics, v. 77, p. 12-15, 1998Tradução . . Acesso em: 19 abr. 2024.
APA
Coêlho, K. -É. F. A., Ramos, E. S., Félix, T. M., Martelli, L. R., Pina Neto, J. M. de, & Niikawa, N. (1998). Three new cases of spondylocarpotarsal synostosis syndrome: clinical and radiographic studies. American Journal of Medical Genetics, 77, 12-15.
NLM
Coêlho K-ÉFA, Ramos ES, Félix TM, Martelli LR, Pina Neto JM de, Niikawa N. Three new cases of spondylocarpotarsal synostosis syndrome: clinical and radiographic studies. American Journal of Medical Genetics. 1998 ; 77 12-15.[citado 2024 abr. 19 ]
Vancouver
Coêlho K-ÉFA, Ramos ES, Félix TM, Martelli LR, Pina Neto JM de, Niikawa N. Three new cases of spondylocarpotarsal synostosis syndrome: clinical and radiographic studies. American Journal of Medical Genetics. 1998 ; 77 12-15.[citado 2024 abr. 19 ]
Artigo de periodico
The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome (1980)
Otto, Paulo A ; Otto, Priscila Guimarães
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: SÍNDROME DE DOWN
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OTTO, Paulo A e OTTO, Priscila Guimarães. The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome. American Journal of Medical Genetics, v. 6, p. 145-152, 1980Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320060208. Acesso em: 19 abr. 2024.
APA
Otto, P. A., & Otto, P. G. (1980). The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome. American Journal of Medical Genetics, 6, 145-152. doi:10.1002/ajmg.1320060208
NLM
Otto PA, Otto PG. The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome [Internet]. American Journal of Medical Genetics. 1980 ; 6 145-152.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320060208
Vancouver
Otto PA, Otto PG. The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome [Internet]. American Journal of Medical Genetics. 1980 ; 6 145-152.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320060208
Artigo de periodico
Teebi hypertelorism syndrome: additional cases (2003)
Paula, Ligiane Alves Machado; Guion-Almeida, Maria Leine
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, HIPERTELORISMO
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ABNT
PAULA, Ligiane Alves Machado e GUION-ALMEIDA, Maria Leine. Teebi hypertelorism syndrome: additional cases. American Journal of Medical Genetics, v. 117A, n. 2, p. 181-183, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10919. Acesso em: 19 abr. 2024.
APA
Paula, L. A. M., & Guion-Almeida, M. L. (2003). Teebi hypertelorism syndrome: additional cases. American Journal of Medical Genetics, 117A( 2), 181-183. doi:10.1002/ajmg.a.10919
NLM
Paula LAM, Guion-Almeida ML. Teebi hypertelorism syndrome: additional cases [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 2): 181-183.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.10919
Vancouver
Paula LAM, Guion-Almeida ML. Teebi hypertelorism syndrome: additional cases [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 2): 181-183.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.10919
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: 19 abr. 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 abr. 19 ]
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 abr. 19 ]
Artigo de periodico
Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a Brazilian family [Brief clinical report] (1983)
Richieri-Costa, Antonio; Gollop, Thomaz Rafael; Colleto, G. M. D. D.
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: DISOSTOSE CRÂNIOFACIAL, FISSURA LÁBIOPALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e GOLLOP, Thomaz Rafael e COLLETO, G. M. D. D. Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a Brazilian family [Brief clinical report]. American Journal of Medical Genetics, v. 14, n. 2, p. 225-229, 1983Tradução . . Acesso em: 19 abr. 2024.
APA
Richieri-Costa, A., Gollop, T. R., & Colleto, G. M. D. D. (1983). Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a Brazilian family [Brief clinical report]. American Journal of Medical Genetics, 14( 2), 225-229.
NLM
Richieri-Costa A, Gollop TR, Colleto GMDD. Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a Brazilian family [Brief clinical report]. American Journal of Medical Genetics. 1983 ; 14( 2): 225-229.[citado 2024 abr. 19 ]
Vancouver
Richieri-Costa A, Gollop TR, Colleto GMDD. Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a Brazilian family [Brief clinical report]. American Journal of Medical Genetics. 1983 ; 14( 2): 225-229.[citado 2024 abr. 19 ]
Artigo de periodico
Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis (1998)
Rabbi-Bortolini, Eliete; Bernardino, Andréa L F; Lopes, Adoris L; Ferri, Adriana da Silva; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RABBI-BORTOLINI, Eliete et al. Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis. American Journal of Medical Genetics, v. 76, p. 288-290, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q. Acesso em: 19 abr. 2024.
APA
Rabbi-Bortolini, E., Bernardino, A. L. F., Lopes, A. L., Ferri, A. da S., Passos-Bueno, M. R., & Zatz, M. (1998). Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis. American Journal of Medical Genetics, 76, 288-290. doi:10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q
NLM
Rabbi-Bortolini E, Bernardino ALF, Lopes AL, Ferri A da S, Passos-Bueno MR, Zatz M. Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis [Internet]. American Journal of Medical Genetics. 1998 ; 76 288-290.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q
Vancouver
Rabbi-Bortolini E, Bernardino ALF, Lopes AL, Ferri A da S, Passos-Bueno MR, Zatz M. Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis [Internet]. American Journal of Medical Genetics. 1998 ; 76 288-290.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q

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