skip to main content
Mostrar Somente
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Material Type:
Artigo de Congresso
Adicionar ao Meu Espaço

Alleles at the rs3212368 SNP at the 3’UTR of the MC1R gene are associated with human pigmentation by possible microRNA influence

L. A. Marano Aguinaldo Luiz Simões; Eduardo Antônio Donadi; Celso Teixeira Mendes Júnior; Annual Meeting of the American Society of Human Genetics (62. 2012 San Francisco)

Abstracts San Francisco: ASHG, 2012

San Francisco ASHG 2012

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2399494 Estantes Deslizantes )(Acessar)

2
Material Type:
Artigo de Congresso
Adicionar ao Meu Espaço

Allelic and genotypic associations of SNPs of the OCA2 and HERC2 genes with eye, hair and skin pigmentation and the presence of freckles in Brazil

E. S. Andrade N. C. A Fracasso; P. S Strazza Júnior; Aguinaldo Luiz Simões; Celso Teixeira Mendes Júnior; Annual Meeting of the American Society of Human Genetics (62. 2012 San Francisco)

Abstracts San Francisco: ASHG, 2012

San Francisco ASHG 2012

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2399521 Estantes Deslizantes )(Acessar)

3
Material Type:
Artigo de Congresso
Adicionar ao Meu Espaço

Complex phenotype associated with 17q21.31 microdeletion

A. Pic Taylor H. Dornelles Wawruk; Carla Rosenberg; Ana Cristina Victorino Krepischi; H.P.N Safatle; L Ferrari; J.F Mazzeu; Annual Meeting of the American Society of Human Genetics 62 2012 San Francisco

Posters: Cytogenetics San Francisco: ASHG, 2012

São Francisco 2012

Acesso online

4
Material Type:
Artigo de Congresso
Adicionar ao Meu Espaço

Array-CGH analysis in patients with Goldenhar Syndrome

S. Sánchez E.L Freitas; H.P.N Safatle; Carla Rosenberg; L Ferrari; S.F Oliveira; J.F Mazzeu; Annual Meeting of the American Society of Human Genetics 62 2012 San Francisco

Posters: Cytogenetics San Francisco: ASHG, 2012

São Francisco 2012

Acesso online

5
Material Type:
Artigo de Congresso
Adicionar ao Meu Espaço

Whole-genome array-CGH screening in patients with autosomal dominant sensorineural hearing loss points to novel susceptibility loci

E.L. Freitas D.T Uehara; V.G.L Dantas; A.G Silva; Ana Cristina Victorino Krepischi; Regina Celia Mingroni Netto; Carla Rosenberg; Annual Meeting of the American Society of Human Genetics 62 2012 San Francisco

Posters: Cytogenetics San Francisco: ASHG, 2012

São Francisco 2012

Acesso online

6
Material Type:
Artigo de Congresso
Adicionar ao Meu Espaço

Association of rare copy number variations and risk for Alzheimer's disease

D. Villela D Schlesinger; Claudia Kimie Suemoto; Lea Tenenholz Grinberg; Ana Cristina Victorino Krepischi; Carla Rosenberg; Annual Meeting of the American Society of Human Genetics 62 2012 San Francisco

Posters: Cytogenetics San Francisco: ASHG, 2012

São Francisco 2012

Acesso online

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (4)
  2. Disponível na Biblioteca (2)

Buscando em bases de dados remotas. Favor aguardar.