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Resultados de 11 a 19 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
11
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:
Artigo de Congresso 		Adicionar ao Meu Espaço

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)

12
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)

13
Evidence for association of the BCL3 gene in 98 Brazilian nonsyndromic clefting patients using the transmission disequilibrium test (TDT)
Evidence for association of the BCL3 gene in 98 Brazilian nonsyndromic clefting patients using the transmission disequilibrium test (TDT)
Material Type:
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Evidence for association of the BCL3 gene in 98 Brazilian nonsyndromic clefting patients using the transmission disequilibrium test (TDT)

D A Gaspar Rita de Cássia M Pavanello; B C Araujo; Márcia André; Silvio Steman; Sergio Russo Matioli; Maria Rita Passos-Bueno; 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. 574, oct. 2001

Chicago 2001

Item não circula. Consulte sua biblioteca.(Acessar)

14
Characterization of TCOF1 mutations in Brazilian patients affected with treacher Collins syndrome
Characterization of TCOF1 mutations in Brazilian patients affected with treacher Collins syndrome
Material Type:
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Characterization of TCOF1 mutations in Brazilian patients affected with treacher Collins syndrome

A Splendore E O Silva; L. G Alonso; Décio Brunoni; Nivaldo Alonso; Antonio Richieri-Costa; D Cavalcanti; Gerson Carakushansky; Mayana Zatz; Maria Rita Passos-Bueno; American Society of Human Genetics (49. 1999 San Francisco)

American Journal of Human Genetics Baltimore v. 65, n. 4, suppl., res.2798, oct. 1999

San Francisco 1999

Item não circula. Consulte sua biblioteca.(Acessar)

15
Recurrent LGMD2A (Calpainopathy) mutations in brazilian patients
Recurrent LGMD2A (Calpainopathy) mutations in brazilian patients
Material Type:
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Recurrent LGMD2A (Calpainopathy) mutations in brazilian patients

F Paula E S Moreira; A L F Bernadino; A Kai; Maria Rita Passos-Bueno; Mariz Vainzof; Mayana Zatz; Annual Meeting of the American Society of Human Genetics (50. 2000 Philadelphia)

American Journal of Human Genetics v. 67, n. 4, suppl. 2, p. 251, Oct. 2000

Chicago 2000

Item não circula. Consulte sua biblioteca.(Acessar)

16
Screening of CFTR and PRSS1 mutations in patients with pancreatitis
Screening of CFTR and PRSS1 mutations in patients with pancreatitis
Material Type:
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Screening of CFTR and PRSS1 mutations in patients with pancreatitis

A L Bernardino D Guarita; C Mott; Marcel Cerqueira César Machado; Antônio Atílio Laudanna; C M Tani; K F Miranda; F L Almeida; Mayana Zatz; Annual Meeting of the American Society of Human Genetics (50. 2000 Philadelphia)

American Journal of Human Genetics v. 67, n. 4, suppl. 2, p. 361 R2018, Oct. 2000

Chicago 2000

Item não circula. Consulte sua biblioteca.(Acessar)

17
Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations
Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations
Material Type:
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Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations

A L F Bernardino A Ferri; Maria Rita Passos-Bueno; C A E Kim; C M A Nakaie; C. E. T Gomes; N Damasceno; American Society of Human Genetics (49. 1999 San Francisco)

American Journal of Human Genetics Baltimore v. 65, n. 4, suppl., res.1164, oct. 1999

San Francisco 1999

Item não circula. Consulte sua biblioteca.(Acessar)

18
Association of specific mutations and severe mental retardation in Duchenne patients
Association of specific mutations and severe mental retardation in Duchenne patients
Material Type:
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Association of specific mutations and severe mental retardation in Duchenne patients

R R Gomes A F B Torres; Mariz Vainzof; A M Cerqueira; Maria Rita Passos-Bueno; Mayana Zatz; American Society of Human Genetics (49. 1999 San Francisco)

American Journal of Human Genetics Baltimore v. 65, n. 4, suppl., res.1671, oct. 1999

San Francisco 1999

Item não circula. Consulte sua biblioteca.(Acessar)

19
Screening of mutations in the Caveolin-3 gene in brazilian limb-girdle muscular dystrophy patients
Screening of mutations in the Caveolin-3 gene in brazilian limb-girdle muscular dystrophy patients
Material Type:
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Screening of mutations in the Caveolin-3 gene in brazilian limb-girdle muscular dystrophy patients

F de Paula Mariz Vainzof; E E McNally; L M Kunkel; Mayana Zatz; American Society of Human Genetics (49. 1999 San Francisco)

American Journal of Human Genetics Baltimore v. 65, n. 4, suppl., res. 2754, oct. 1999

San Francisco 1999

Item não circula. Consulte sua biblioteca.(Acessar)

Resultados de 11 a 19 de 19  para Produção Intelectual da USP

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