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Refinado por: autor: Rosemberg, S remover autor: Suzuki, O remover
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1
Evidence of neuronal migration disorders in knobloch syndrome clinical and molecular analysis of two novel families
Evidence of neuronal migration disorders in knobloch syndrome clinical and molecular analysis of two novel families
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Artigo 		Adicionar ao Meu Espaço

Evidence of neuronal migration disorders in knobloch syndrome clinical and molecular analysis of two novel families

Susana Kliemann Ricardo T. L Waetge; Oscar T Suzuki; Maria Rita Passos-Bueno; Sergio Rosemberg

American Journal of Medical Genetics Reino Unido v. 119 A, n. 1, p. 15-19, 2003

Reino Unido 2003

Localização: FM - Fac. Medicina    (FM-BCBIB )(Acessar)

2
Evidence of neuronal migration disorders in knobloch syndrome clinical and molecular analysis of two novel families
Evidence of neuronal migration disorders in knobloch syndrome clinical and molecular analysis of two novel families
Material Type:
Artigo 		Adicionar ao Meu Espaço

Evidence of neuronal migration disorders in knobloch syndrome clinical and molecular analysis of two novel families

Susana Kliemann Ricardo T. L Waetge; Oscar T Suzuki; Maria Rita Passos-Bueno; Sergio Rosemberg

American Journal of Medical Genetics Reino Unido v. 119 A, n. 1, p. 15-19, 2003

Reino Unido 2003

Localização: FM - Fac. Medicina    (FM-BCBIB )(Acessar)

3
Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome
Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome

Oscar T. Suzuki Andréa Laurato Sertié; Vazken M Der Kaloustian; Fernando Kok; M Carpenter; J Murray; A E Czeizel; Susana E Kliemann; Sérgio Rosemberg; M Monteiro; Bjorn Reino Olsen; Maria Rita Passos-Bueno

American Journal of Human Genetics v. 71, p. 1320-1329, 2002

Baltimore 2002

Item não circula. Consulte sua biblioteca.(Acessar)

4
Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome
Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome

Oscar T. Suzuki Andréa Laurato Sertié; Vazken M Der Kaloustian; Fernando Kok; M Carpenter; J Murray; A E Czeizel; Susana E Kliemann; Sérgio Rosemberg; M Monteiro; Bjorn Reino Olsen; Maria Rita Passos-Bueno

American Journal of Human Genetics v. 71, p. 1320-1329, 2002

Baltimore 2002

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Rosemberg, S
  2. Suzuki, O
  3. Passos-Bueno, M
  4. Kliemann, S
  5. Kok, F

Neste Assunto:

  1. Doenças Retinianas
  2. Oftalmopatias (Genética)
  3. Cegueira
  4. Anticorpos
  5. Degeneração Retiniana

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

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