ReP USP - Resultado da busca

Artigo de periodico
Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes (2004)
Versiani, Beatriz Ribeiro; Gilbert-Barness, Enid; Giuliani, Liane Rosso; Peres, Luiz César; Pina Neto, João Monteiro de
Source: Clinical Dysmorphology. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VERSIANI, Beatriz Ribeiro et al. Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes. Clinical Dysmorphology, v. 13, p. 1-5, 2004Tradução . . Disponível em: https://doi.org/10.1097/00019605-200401000-00001. Acesso em: 05 nov. 2024.
APA
Versiani, B. R., Gilbert-Barness, E., Giuliani, L. R., Peres, L. C., & Pina Neto, J. M. de. (2004). Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes. Clinical Dysmorphology, 13, 1-5. doi:10.1097/00019605-200401000-00001
NLM
Versiani BR, Gilbert-Barness E, Giuliani LR, Peres LC, Pina Neto JM de. Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes [Internet]. Clinical Dysmorphology. 2004 ; 13 1-5.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1097/00019605-200401000-00001
Vancouver
Versiani BR, Gilbert-Barness E, Giuliani LR, Peres LC, Pina Neto JM de. Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes [Internet]. Clinical Dysmorphology. 2004 ; 13 1-5.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1097/00019605-200401000-00001
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: 05 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. 05 ] 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. 05 ] Available from: https://doi.org/10.1097/00019605-200304000-00015
Artigo de periodico
Raine dysplasia: a brazilian case with a mild radiological involvement (2000)
Acosta, A. X.; Peres, Luiz César; Chimelli, L. C.; Pina Neto, João Monteiro de
Source: Clinical Dysmorphology. Unidade: FMRP
Subjects: DOENÇAS ÓSSEAS, TRANSTORNOS CEREBROVASCULARES, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ACOSTA, A. X. et al. Raine dysplasia: a brazilian case with a mild radiological involvement. Clinical Dysmorphology, v. 9, n. 2, p. 99-101, 2000Tradução . . Disponível em: https://doi.org/10.1097/00019605-200009020-00004. Acesso em: 05 nov. 2024.
APA
Acosta, A. X., Peres, L. C., Chimelli, L. C., & Pina Neto, J. M. de. (2000). Raine dysplasia: a brazilian case with a mild radiological involvement. Clinical Dysmorphology, 9( 2), 99-101. doi:10.1097/00019605-200009020-00004
NLM
Acosta AX, Peres LC, Chimelli LC, Pina Neto JM de. Raine dysplasia: a brazilian case with a mild radiological involvement [Internet]. Clinical Dysmorphology. 2000 ; 9( 2): 99-101.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1097/00019605-200009020-00004
Vancouver
Acosta AX, Peres LC, Chimelli LC, Pina Neto JM de. Raine dysplasia: a brazilian case with a mild radiological involvement [Internet]. Clinical Dysmorphology. 2000 ; 9( 2): 99-101.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1097/00019605-200009020-00004
Artigo de periodico
Syndrome of psychomotor retardation, bulbous nose, and epilepsy (hernandez syndrome): a Brazilian case (1999)
Melo, Débora Gusmão; Acosta, Angelina Xavier; Pina Neto, João Monteiro de
Source: Clinical Dysmorphology. Unidade: FMRP
Subjects: TRANSTORNOS MENTAIS (EPIDEMIOLOGIA), OBESIDADE, EPILEPSIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, Débora Gusmão e ACOSTA, Angelina Xavier e PINA NETO, João Monteiro de. Syndrome of psychomotor retardation, bulbous nose, and epilepsy (hernandez syndrome): a Brazilian case. Clinical Dysmorphology, v. 8, n. 4, p. 301-303, 1999Tradução . . Acesso em: 05 nov. 2024.
APA
Melo, D. G., Acosta, A. X., & Pina Neto, J. M. de. (1999). Syndrome of psychomotor retardation, bulbous nose, and epilepsy (hernandez syndrome): a Brazilian case. Clinical Dysmorphology, 8( 4), 301-303.
NLM
Melo DG, Acosta AX, Pina Neto JM de. Syndrome of psychomotor retardation, bulbous nose, and epilepsy (hernandez syndrome): a Brazilian case. Clinical Dysmorphology. 1999 ; 8( 4): 301-303.[citado 2024 nov. 05 ]
Vancouver
Melo DG, Acosta AX, Pina Neto JM de. Syndrome of psychomotor retardation, bulbous nose, and epilepsy (hernandez syndrome): a Brazilian case. Clinical Dysmorphology. 1999 ; 8( 4): 301-303.[citado 2024 nov. 05 ]
Artigo de periodico
The X-linked mental retardation, macrosomia, macrocephaly and obesity syndrome (Baraitser syndrome): a Brazilian case (1998)
Pina Neto, João Monteiro de; Molfetta, Greice Andreotti de
Source: Clinical Dysmorphology. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINA NETO, João Monteiro de e MOLFETTA, Greice Andreotti de. The X-linked mental retardation, macrosomia, macrocephaly and obesity syndrome (Baraitser syndrome): a Brazilian case. Clinical Dysmorphology, v. 7, n. 1, p. 1-2, 1998Tradução . . Disponível em: https://doi.org/10.1097/00019605-199807000-00017. Acesso em: 05 nov. 2024.
APA
Pina Neto, J. M. de, & Molfetta, G. A. de. (1998). The X-linked mental retardation, macrosomia, macrocephaly and obesity syndrome (Baraitser syndrome): a Brazilian case. Clinical Dysmorphology, 7( 1), 1-2. doi:10.1097/00019605-199807000-00017
NLM
Pina Neto JM de, Molfetta GA de. The X-linked mental retardation, macrosomia, macrocephaly and obesity syndrome (Baraitser syndrome): a Brazilian case [Internet]. Clinical Dysmorphology. 1998 ; 7( 1): 1-2.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1097/00019605-199807000-00017
Vancouver
Pina Neto JM de, Molfetta GA de. The X-linked mental retardation, macrosomia, macrocephaly and obesity syndrome (Baraitser syndrome): a Brazilian case [Internet]. Clinical Dysmorphology. 1998 ; 7( 1): 1-2.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1097/00019605-199807000-00017

USP Schools

ReP

Filtros

Authors

Subjects

Indexado em