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Refinado por: Nome da Publicação: American Journal of Medical Genetics remover assunto: Malformações remover
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1
Further evidence for a fourth gene causing X-linked pure spastic paraplegia
Further evidence for a fourth gene causing X-linked pure spastic paraplegia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Further evidence for a fourth gene causing X-linked pure spastic paraplegia

A. Starling P Rocco; F Cambi; G. M Hobson; Maria Rita Passos-Bueno; Mayana Zatz

American Journal of Medical Genetics v. 111, p. 152-156, 2002

New York 2002

Item não circula. Consulte sua biblioteca.(Acessar)

2
Further evidence for a fourth gene causing X-linked pure spastic paraplegia
Further evidence for a fourth gene causing X-linked pure spastic paraplegia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Further evidence for a fourth gene causing X-linked pure spastic paraplegia

A. Starling P Rocco; F Cambi; G. M Hobson; Maria Rita Passos-Bueno; Mayana Zatz

American Journal of Medical Genetics v. 111, p. 152-156, 2002

New York 2002

Item não circula. Consulte sua biblioteca.(Acessar)

3
Origin of uniparental disomy 15 in patients with Prader-Willi or Algelman Syndrome
Origin of uniparental disomy 15 in patients with Prader-Willi or Algelman Syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Origin of uniparental disomy 15 in patients with Prader-Willi or Algelman Syndrome

Cintia Fridman Celia Priszkulnik Koiffmann

American Journal of Medical Genetics v. 94, p. 249-253, 2000

New York 2000

Acesso online

4
Origin of uniparental disomy 15 in patients with Prader-Willi or Algelman Syndrome
Origin of uniparental disomy 15 in patients with Prader-Willi or Algelman Syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Origin of uniparental disomy 15 in patients with Prader-Willi or Algelman Syndrome

Cintia Fridman Célia Priszkulnik Koiffmann

American Journal of Medical Genetics v. 94, p. 249-253, 2000

New York 2000

Acesso online

5
Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate results From a Case-Control Study in Brazil. [Carta]
Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate results From a Case-Control Study in Brazil. [Carta]
Material Type:
Artigo 		Adicionar ao Meu Espaço

Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate results From a Case-Control Study in Brazil. [Carta]

D A Gaspar R.C Pavanello; Mayana Zatz; Maria Rita Passos-Bueno; M Andre; S Steman; D. F Wyszynski; Sergio Russo Matioli

American Journal of Medical Genetics Hoboken v. 87, p. 197-199, 1999

Hoboken 1999

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Passos-Bueno, M
  2. Zatz, M
  3. Rocco, P
  4. Hobson, G
  5. Cambi, F

Neste Assunto:

  1. Genética Médica
  2. Doenças Hereditárias
  3. Síndrome De Angelman
  4. Mutação Genética
  5. Polimorfismo

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

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