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1
Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes
Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes
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Artigo 		Adicionar ao Meu Espaço

Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes

Steven B. Bleyl Janice L. B Byrne; Sarah T South; David C Dries; David A Stevenson; Alan F Rope; Angela M Vianna-Morgante; Gary C Schoenwolf; Jane D Kivlin; Arthur Brothman; John C Carey

American Journal of Medical Genetics. Part A v. 143A, n. 23, p. 2785-2795, 2007

Hoboken 2007

Item não circula. Consulte sua biblioteca.(Acessar)

2
Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes
Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes
Material Type:
Artigo 		Adicionar ao Meu Espaço

Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes

Steven B. Bleyl Janice L. B Byrne; Sarah T South; David C Dries; David A Stevenson; Alan F Rope; Angela Maria Vianna-Morgante; Gary C Schoenwolf; Jane D Kivlin; Arthur Brothman; John C Carey

American Journal of Medical Genetics. Part A v. 143A, n. 23, p. 2785-2795, 2007

Hoboken 2007

Item não circula. Consulte sua biblioteca.(Acessar)

3
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair
Material Type:
Artigo 		Adicionar ao Meu Espaço

Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair

Marijke Bauters Hilde Van Esch; Michael J Friez; Odile Boespflug-Tanguy; Martin Zenker; Angela M Vianna-Morgante; Carla Rosenberg; Jaakko Ignatius; Martine Raynaud; Karen Hollanders; Karen Govaerts; Kris Vandenreijt; Florence Niel; Pierre Blanc; Roger E Stevenson; Jean-Pierre Fryns; Peter Marynen; Charles E Schwartz; Guy Froyen

Genome Research v. 18, p. 847-858, 2008

Woodbury 2008

Item não circula. Consulte sua biblioteca.(Acessar)

4
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair
Material Type:
Artigo 		Adicionar ao Meu Espaço

Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair

Marijke Bauters Hilde Van Esch; Michael J Friez; Odile Boespflug-Tanguy; Martin Zenker; Angela Maria Vianna-Morgante; Carla Rosenberg; Jaakko Ignatius; Martine Raynaud; Karen Hollanders; Karen Govaerts; Kris Vandenreijt; Florence Niel; Pierre Blanc; Roger E Stevenson; Jean-Pierre Fryns; Peter Marynen; Charles E Schwartz; Guy Froyen

Genome Research v. 18, p. 847-858, 2008

Woodbury 2008

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Vianna-Morgante, A
  2. Blanc, P
  3. Dries, D
  4. Niel, F
  5. Van Esch, H

Neste Assunto:

  1. Doenças Genéticas
  2. Retardo Mental
  3. Anormalidades Cromossômicas

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

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