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1
ROR1 gene is mutated in the dominant form of Robinow syndrome
ROR1 gene is mutated in the dominant form of Robinow syndrome
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

ROR1 gene is mutated in the dominant form of Robinow syndrome

Angela Maria Vianna-Morgante H. G Brunner; H Van Bokhoven; B Hamel; Juliana Forte Mazzeu; Annual Meeting of the American Society of Human Genetics (52. 2002 Baltimore)

Abstracts v. 71, n. 4, suppl., p. 539 res.2164, oct. 2002

Baltimore 2002

Item não circula. Consulte sua biblioteca.(Acessar)

2
A mutation in the CCAAT box of the TERC promoter region causes telomere disease
A mutation in the CCAAT box of the TERC promoter region causes telomere disease
Material Type:
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A mutation in the CCAAT box of the TERC promoter region causes telomere disease

Anna M. Aalbers Sachiko Kajigaya; Marry M. van den Heuvel; Vincent van der Velden; Michel Zwaan; Rob Pieters; Rodrigo T Calado; Neal S Young; Meeting of the Telomeres & Telomerase (2011 New York)

Abstracts New York

New York 2011

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2255618 estantes deslizantes ) e outros locais(Acessar)

3
Analysis of five genes in brazilian patients with nonsyndromic mental retardation
Analysis of five genes in brazilian patients with nonsyndromic mental retardation
Material Type:
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Analysis of five genes in brazilian patients with nonsyndromic mental retardation

Carlos Magno da Costa Maranduba Angela M Vianna-Morgante; Maria Rita Passos-Bueno; Annual Meeting of the American Society of Human Genetics (54. 2004 Toronto)

Abstracts Toronto, 2004

Toronto 2004

Item não circula. Consulte sua biblioteca.(Acessar)

4
Screening of patients with trigonocephaly with markers from the 9p and 11q regions
Screening of patients with trigonocephaly with markers from the 9p and 11q regions
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Screening of patients with trigonocephaly with markers from the 9p and 11q regions

Fernanda Sarquis Jehee D Johnson; L Alonso; K Abe; N Alonso; Hamilton Matushita; C Kim; S Cavalheiro; S. A Wall; A. O. M Wilkie; Maria Rita Passos-Bueno; Annual Meeting of the American Society of Human Genetics (52. 2002 Baltimore)

Abstracts v. 71, n. 4, suppl., p. 514 res.2017, oct. 2002

Baltimore 2002

Item não circula. Consulte sua biblioteca.(Acessar)

5
Expression and functional gene analysis in periosteal fibroblasts from Apert syndrome patients
Expression and functional gene analysis in periosteal fibroblasts from Apert syndrome patients
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Expression and functional gene analysis in periosteal fibroblasts from Apert syndrome patients

Andréa Laurato Sertié R. D Fanganiello; N Oliveira; Sérgio Cavalheiro; N Alonso; Maria Rita Passos-Bueno; Annual Meeting of the American Society of Human Genetics (54. 2004 Toronto)

Abstracts Toronto, 2004

Toronto 2004

Item não circula. Consulte sua biblioteca.(Acessar)

6
The Treacher Collins syndrome gene (TCOF1) promoter characterization
The Treacher Collins syndrome gene (TCOF1) promoter characterization
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

The Treacher Collins syndrome gene (TCOF1) promoter characterization

C Masotti L. M Annelin-Correa; Alessandra Splendore; A Barbosa; C. J Lins; S Brochado; Têmis Maria Félix; Mari Cleide Sogayar; Maria Rita Passos-Bueno; Annual Meeting of the American Society of Human Genetics (54. 2004 Toronto)

Abstracts Toronto, 2004

Toronto 2004

Item não circula. Consulte sua biblioteca.(Acessar)

7
Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients
Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients
Material Type:
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Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients

C. Varela Fernando Kok; Nuvarte Setian; C A Kim; Célia Priszkulnik Koiffmann; Annual Meeting of the American Society of Human Genetics (54. 2004 Toronto, Canadá)

Abstracts Toronto, 2004

Toronto 2004

Item não circula. Consulte sua biblioteca.(Acessar)

8
Identification of novel men1 germline mutations and genetic screening in brazilian families with multiple endocrine neoplasia type
Identification of novel men1 germline mutations and genetic screening in brazilian families with multiple endocrine neoplasia type
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Identification of novel men1 germline mutations and genetic screening in brazilian families with multiple endocrine neoplasia type

R. A. Toledo D. M Lourenço Junior; F. L Coutinho; S. P. A Toledo; Reunião Anual da Federação de Sociedades de Biologia Experimental(FeSBE) (22. 2007 Águas de Lindóia)

Abstracts São Paulo : FeSBE, 2007

São Paulo FeSBE 2007

Acesso online. A biblioteca também possui exemplares impressos.

9
Studies of protein interactions and stability of Sdo1p
Studies of protein interactions and stability of Sdo1p
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Studies of protein interactions and stability of Sdo1p

A. Z. N Fernandes Cleslei Fernando Zanelli; S R Valentini; Carla Columbano de Oliveira; J. S Luiz; Annual Meeting of the Brazilian Biochemistry and Molecular Biology Society (SBBq) (42. 2013 Foz do Iguaçu)

Abstracts São Paulo : Sociedade Brasileira de Bioquímica e Biologia Molecular (SBBq), 2013

São Paulo Sociedade Brasileira de Bioquímica e Biologia Molecular SBBq 2013

Item não circula. Consulte sua biblioteca.(Acessar)

10
Comparative genomic analysis of colorectal cancer
Comparative genomic analysis of colorectal cancer
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Comparative genomic analysis of colorectal cancer

A. S. Fonseca M. C Burger; Jorge Estéfano Santana de Souza; K. A Silva; C. P Alves; D. L Zanette; Fernanda Maris Peria; Omar Feres; José Joaquim Ribeiro da Rocha; A. R Dinarte; Amélia Goes Araújo; R. A Panepucci; Wilson Araújo da Silva Júnior; Workshop do Programa de Pós-Graduação em Genética FMRP-USP (4. 2013 Ribeirão Preto)

Resumos Ribeirão Preto : FMRP-USP, 2013

Ribeirão Preto FMRP-USP 2013

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2462824 Estantes Deslizantes ) e outros locais(Acessar)

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