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New molecular mechanism for ullrich congenital muscular dystrophy a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype
New molecular mechanism for ullrich congenital muscular dystrophy a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype
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New molecular mechanism for ullrich congenital muscular dystrophy a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype

Te-Cheng Pan Rui Zhu Zhang; Dominick G Sudano; Suely K Marie; Carsten G Bonnemann; Mon Li Chu

American Journal of Human Genetics Chicago v. 73, p. 355-369, 2003

Chicago 2003

Localização: FM - Fac. Medicina    (FM BCSEP 2003 253 )(Acessar)

2
New molecular mechanism for ullrich congenital muscular dystrophy a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype
New molecular mechanism for ullrich congenital muscular dystrophy a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype
Material Type:
Artigo 		Adicionar ao Meu Espaço

New molecular mechanism for ullrich congenital muscular dystrophy a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype

Te-Cheng Pan Rui Zhu Zhang; Dominick G Sudano; Suely K Marie; Carsten G Bonnemann; Mon Li Chu

American Journal of Human Genetics Chicago v. 73, p. 355-369, 2003

Chicago 2003

Localização: FM - Fac. Medicina    (FM BCSEP 2003 253 )(Acessar)

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Deste Autor:

  1. Pan, T
  2. Marie, S
  3. Sudano, D
  4. Zhang, R
  5. Bonnemann, C

Neste Assunto:

  1. Distrofia Muscular
  2. Fenótipos
  3. Deleção De Genes
  4. Mutação Genética

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

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