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Resultados de 1 a 10 de 19  para Produção Intelectual da USP

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Refinado por: Nome da Publicação: American Journal of Human Genetics remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
The recurrent basque mutation in Brazilian calpainopathy patients
The recurrent basque mutation in Brazilian calpainopathy patients
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

The recurrent basque mutation in Brazilian calpainopathy patients

F de Paula A Sáenz; A. M Cobo; A Lopez de Munain; A Urtizberea; Annual Meeting of the American Society of Human Genetics (53. 2003 Los Angeles)

American Journal of Human Genetics Baltimore v. 73, n. 5, suppl., p. 580, 2003

Baltimore 2003

Item não circula. Consulte sua biblioteca.(Acessar)

2
Molecular and cytogenetic analyses in Brazilian patients affected by autism spectrum disorders
Molecular and cytogenetic analyses in Brazilian patients affected by autism spectrum disorders
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Molecular and cytogenetic analyses in Brazilian patients affected by autism spectrum disorders

E. S. Moreira G. M Orabona; L. O Avelar; E Vadasz; L. M Biason; V. N. O Takahashi; K Abe; Angela Maria Vianna-Morgante; Maria Rita Passos-Bueno; Annual Meeting of the American Society of Human Genetics (53. 2003 Los Angeles)

American Journal of Human Genetics Baltimore v. 73, n. 5, suppl., p. 520, nov. 2003

Baltimore 2003

Item não circula. Consulte sua biblioteca.(Acessar)

3
Analysis of the interleukin-1 gene complex in LOAD brazilian patients
Analysis of the interleukin-1 gene complex in LOAD brazilian patients
Material Type:
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Analysis of the interleukin-1 gene complex in LOAD brazilian patients

Agnes L. Nishimura F. B Mury; M Mitne-Neto; J. R. M Oliveira; Ricardo Nitrini; Valéria Santoro Bahia; Paulo Roberto Brito-Marques; M Neri; S. M. M Fertuzinhos; Mayana Zatz; Annual Meeting of the American Society of Human Genetics (53. 2003 Los Angeles)

American Journal of Human Genetics Baltimore v. 73, n. 5, supl., p. 468, 2003

Baltimore 2003

Item não circula. Consulte sua biblioteca.(Acessar)

4
Muscle proteins alteration in patients with mutations in the Fukutin-Related protein gene
Muscle proteins alteration in patients with mutations in the Fukutin-Related protein gene
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Muscle proteins alteration in patients with mutations in the Fukutin-Related protein gene

L. U. Yamamoto Marta Canovas; Rita de Cássia M Pavanello; B. L Lima; F de Paula; N Vieira; Mayana Zatz; Mariz Vainzof; Annual Meeting of the American Society of Human Genetics (53. 2003 Los Angeles)

American Journal of Human Genetics Baltimore v. 73, n. 5, suppl., p. 556, 2003

2003

Item não circula. Consulte sua biblioteca.(Acessar)

5
Phenotype and behavior in patients with Algelman syndrome comparisons between the different classes of deletions and between patients with a deletion and with UPD
Phenotype and behavior in patients with Algelman syndrome comparisons between the different classes of deletions and between patients with a deletion and with UPD
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Phenotype and behavior in patients with Algelman syndrome comparisons between the different classes of deletions and between patients with a deletion and with UPD

M. C. Varela Fernando Kok; I Kohl; C. I. E Castro; Célia Priszkulnik Koiffmann; Annual Meeting of the American Society of Human Genetics (53. 2003 Los Angeles)

American Journal of Human Genetics v. 73, n. 5, suppl., p. 319, 2003

Baltimore 2003

Item não circula. Consulte sua biblioteca.(Acessar)

6
Alcohol dehydrogenase 4 polymorphisms as a risk factor for alcoholism in Brazilian patients
Alcohol dehydrogenase 4 polymorphisms as a risk factor for alcoholism in Brazilian patients
Material Type:
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Alcohol dehydrogenase 4 polymorphisms as a risk factor for alcoholism in Brazilian patients

Mayana Zatz Camila Guindalini; Sandra Scivoletto; R. G. M Ferreira; G Breen; M Ziberman; M. A Peluso; Elisangela Quedas; Agnes L Nishimura; Annual Meeting of the American Society of Human Genetics (53. 2003 Los Angeles)

American Journal of Human Genetics Baltimore v. 73, n. 5, suppl., p. 524, 2003

Baltimore 2003

Item não circula. Consulte sua biblioteca.(Acessar)

7
Novel dysferlin mutations in brazilian LGMD2B patients
Novel dysferlin mutations in brazilian LGMD2B patients
Material Type:
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Novel dysferlin mutations in brazilian LGMD2B patients

F. Paula Mariz Vainzof; E. S Moreira; Maria Rita Passos-Bueno; K Bushby; Rumaisa Bashir; Mayana Zatz; Annual Meeting of the American Society of Human Genetics (51. 2001 San Diego)

American Journal of Human Genetics Chicago v. 69, n. 4, suppl., p. 639, oct. 2001

Chicago 2001

Item não circula. Consulte sua biblioteca.(Acessar)

8
Mutation analysis of UBE3A gene in Angelman syndrome patients
Mutation analysis of UBE3A gene in Angelman syndrome patients
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Mutation analysis of UBE3A gene in Angelman syndrome patients

G. A. Molfetta W. A Silva Júnior; J Wagstalf; João Monteiro de Pina Neto; Annual Meeting of the American Journal of Human Genetics (2001 Chicago)

American Journal of Human Genetics Chicago v. 69, n. 4, p. 580 res. 2345, 2001

Chicago 2001

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1226236 ) e outros locais(Acessar)

9
Associated factors evaluation in recurrent and/or severe infections in Down's syndrome patients
Associated factors evaluation in recurrent and/or severe infections in Down's syndrome patients
Material Type:
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Associated factors evaluation in recurrent and/or severe infections in Down's syndrome patients

L. M. A. Ribeiro A. C Pastorino; Chong Ae Kim; A. P. M Castro; A. B. F Fomin; Cristina Miuki Abe Jacob; Annual Meeting (2001 Chicago)

American Journal Of Human Genetics Chicago v. 69, n. 4, supl. , res. 666, 2001

Chicago 2001

Item não circula. Consulte sua biblioteca.(Acessar)

10
Six novel point mutations in the dystrophin gene identified in Brazilian Duchenne patients
Six novel point mutations in the dystrophin gene identified in Brazilian Duchenne patients
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Six novel point mutations in the dystrophin gene identified in Brazilian Duchenne patients

Dulci do Nascimento Fonseca Vagenas A Cerqueira; A Torres; Rita de Cássia M Pavanello; Maria Rita Passos-Bueno; Mayana Zatz; Annual Meeting of the American Society of Human Genetics (51. 2001 San Diego)

American Journal of Human Genetics v. 69, n. 4, suppl., p. 442, oct. 2001

Chicago 2001

Item não circula. Consulte sua biblioteca.(Acessar)

Resultados de 1 a 10 de 19  para Produção Intelectual da USP

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