skip to main content
Idioma:
Você quis dizer: maria m?
Resultados 1 2 3 4 5 next page
Mostrar Somente
Refinado por: Nome da Publicação: American Journal of Medical Genetics remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Classification and birth prevalence of orofacial clefts
Classification and birth prevalence of orofacial clefts
Material Type:
Artigo 		Adicionar ao Meu Espaço

Classification and birth prevalence of orofacial clefts

Tolarová, Marie M. ; Cervenka, Jaroslav

American journal of medical genetics, 1998-01, Vol.75 (2), p.126-137 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

Texto completo disponível

Citações Citado por
2
Knobloch syndrome in a large brazilian consanguineous family confirmation of autosomal recessive inheritance
Knobloch syndrome in a large brazilian consanguineous family confirmation of autosomal recessive inheritance
Material Type:
Artigo 		Adicionar ao Meu Espaço

Knobloch syndrome in a large brazilian consanguineous family confirmation of autosomal recessive inheritance

Maria Rita Passos-Bueno Suely Kazue Nagahashi Marie; M Monteiro; I Neustein; M R Whittle; M Vainzof; M Zatz

New York v.52, n.2 , p.170-3, aug. 1994 American Journal of Medical Genetics

New York 1994

Item não circula. Consulte sua biblioteca.(Acessar)

3
Racial and ethnic variations in the prevalence of orofacial clefts in California, 1983-1992
Racial and ethnic variations in the prevalence of orofacial clefts in California, 1983-1992
Material Type:
Artigo 		Adicionar ao Meu Espaço

Racial and ethnic variations in the prevalence of orofacial clefts in California, 1983-1992

Croen, Lisa A. ; Shaw, Gary M. ; Wasserman, Cathy R. ; Tolarová, Marie M.

American journal of medical genetics, 1998-08, Vol.79 (1), p.42-47 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

Texto completo disponível

Citações Citado por
4
Knobloch syndrome in a large brazilian consanguineous family confirmation of autosomal recessive inheritance
Knobloch syndrome in a large brazilian consanguineous family confirmation of autosomal recessive inheritance
Material Type:
Artigo 		Adicionar ao Meu Espaço

Knobloch syndrome in a large brazilian consanguineous family confirmation of autosomal recessive inheritance

Maria Rita Passos-Bueno Suely Kazue Nagahashi Marie; M Monteiro; I Neustein; M R Whittle; Mariz Vainzof; Mayana Zatz

New York v.52, n.2 , p.170-3, aug. 1994 American Journal of Medical Genetics

New York 1994

Item não circula. Consulte sua biblioteca.(Acessar)

5
Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families
Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families
Material Type:
Artigo 		Adicionar ao Meu Espaço

Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families

Paula Iughetti Paulo A Otto; Mayana Zatz; Maria Rita Passos-Bueno; Suely Kazue Nagahashi Marie

American Journal of Medical Genetics v. 77, n. 3, p. 246-248, 1998

Hoboken 1998

Item não circula. Consulte sua biblioteca.(Acessar)

6
Maternal periconceptional use of multivitamins and reduced risk for conotruncal heart defects and limb deficiencies among offspring
Maternal periconceptional use of multivitamins and reduced risk for conotruncal heart defects and limb deficiencies among offspring
Material Type:
Artigo 		Adicionar ao Meu Espaço

Maternal periconceptional use of multivitamins and reduced risk for conotruncal heart defects and limb deficiencies among offspring

Shaw, Gary M. ; O'Malley, Cynthia D. ; Wasserman, Cathy R. ; Tolarova, Marie M. ; Lammer, Edward J.

American journal of medical genetics, 1995-12, Vol.59 (4), p.536-545 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

Texto completo disponível

Citações Citado por
7
Birth prevalence, mutation rate, sex ratio, parents' age, and ethnicity in Apert syndrome
Birth prevalence, mutation rate, sex ratio, parents' age, and ethnicity in Apert syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Birth prevalence, mutation rate, sex ratio, parents' age, and ethnicity in Apert syndrome

Tolarova, Marie M. ; Harris, John A. ; Ordway, Doris E. ; Vargervik, Karin

American journal of medical genetics, 1997-11, Vol.72 (4), p.394-398 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

Texto completo disponível

Citações Citado por
8
Association between the dopamine receptor D4 (DRD4) gene and obsessive-compulsive disorder
Association between the dopamine receptor D4 (DRD4) gene and obsessive-compulsive disorder
Material Type:
Artigo 		Adicionar ao Meu Espaço

Association between the dopamine receptor D4 (DRD4) gene and obsessive-compulsive disorder

Millet, Bruno ; Chabane, Nadia ; Delorme, Richard ; Leboyer, Marion ; Leroy, Sophie ; Poirier, Marie-France ; Bourdel, Marie-Chantal ; Mouren-Simeoni, Marie-Christine ; Rouillon, Fréderic ; Loo, Henri ; Krebs, Marie-Odile

American journal of medical genetics, 2003-01, Vol.116B (1), p.55-59 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

Texto completo disponível

Citações Citado por
9
Periconceptional intake of vitamin supplements and risk of multiple congenital anomalies
Periconceptional intake of vitamin supplements and risk of multiple congenital anomalies
Material Type:
Artigo 		Adicionar ao Meu Espaço

Periconceptional intake of vitamin supplements and risk of multiple congenital anomalies

Shaw, Gary M. ; Croen, Lisa A. ; Todoroff, Karen ; Tolarova, Marie M.

American journal of medical genetics, 2000-07, Vol.93 (3), p.188-193 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

Texto completo disponível

Citações Citado por
10
Prenatal diagnosis of nail-patella syndrome by intrauterine kidney biopsy
Prenatal diagnosis of nail-patella syndrome by intrauterine kidney biopsy
Material Type:
Artigo 		Adicionar ao Meu Espaço

Prenatal diagnosis of nail-patella syndrome by intrauterine kidney biopsy

Gubler, Marie-Claire ; Levy, Micheline

American journal of medical genetics, 1993-08, Vol.47 (1), p.122-123 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

Texto completo disponível

Citações Citado por
Resultados 1 2 3 4 5 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (339)
  2. Revistas revisadas por pares (308)

Refinar Meus Resultados

Tipo de Recurso 

  1. Artigos  (343)
  2. Resenhas  (1)
  3. Mais opções open sub menu

Data de Publicação 

De até
Refinar
  1. Antes de1986  (13)
  2. 1986Até1990  (30)
  3. 1991Até1995  (65)
  4. 1996Até2001  (147)
  5. Após 2001  (90)
  6. Mais opções open sub menu

Novas Pesquisas Sugeridas

Ignorar minha busca e procurar por tudo

Deste Autor:

  1. Marie, S
  2. Passos-Bueno, M
  3. Zatz, M
  4. Vainzof, M
  5. Otto, P

Neste Assunto:

  1. Humans
  2. Genetics & Heredity
  3. Life Sciences & Biomedicine
  4. Science & Technology
  5. Biological And Medical Sciences

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.