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Refinado por: autor: Rosenberg, C remover autor: Vianna-Morgante, A remover
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1
Inativacao do x fragil e a manifestacao do retardado mental nas heterozigotas
Inativacao do x fragil e a manifestacao do retardado mental nas heterozigotas
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Inativacao do x fragil e a manifestacao do retardado mental nas heterozigotas

C Rosenberg Angela Maria Vianna-Morgante; Paulo Alberto Otto; Congresso Nacional de Genetica (36. 1990 Caxambu); Workshop Latino-Americano da Associacao Latino-Americana de Mutagenese, Carcinogenese e Teratogenese Ambiental-Alamcta (1. 1990 Caxambu)

Programa e Resumos Ribeirão Preto : Sociedade Brasileira de Genetica, 1990

Ribeirao Preto Sociedade Brasileira de Genetica 1990

Item não circula. Consulte sua biblioteca.(Acessar)

2
Translocacoes cromossomicas familiais complexas
Translocacoes cromossomicas familiais complexas
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Translocacoes cromossomicas familiais complexas

C I E Castro C Rosenberg; Aron Judka Diament; Angela Maria Vianna-Morgante; C. P Koiffmann; Congresso Nacional de Genetica (41. 1995 Caxambu)

v.18, n.3 suppl., p.505, sep. 1995 Revista Brasileira de Genetica = Brazilian Journal of Genetics

1995

Localização: FM - Fac. Medicina    (BCSEP 1995 063 ) e outros locais(Acessar)

3
Homozygous duplication at 10p11.21 in a boy clinical manifestations of Lin-Gettig syndrome
Homozygous duplication at 10p11.21 in a boy clinical manifestations of Lin-Gettig syndrome
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Homozygous duplication at 10p11.21 in a boy clinical manifestations of Lin-Gettig syndrome

Juliana Forte Mazzeu Feng Zhang; C M Carvalho; Ana Cristina Victorino Krepischi; S Yatsenko; Eliete Pardono; Paulo Alberto Otto; Carla Rosenberg; J Lupsski; Angela Maria Vianna-Morgante; Annual Meeting of the American Society of Human Genetics (60. 2010 Washington)

Poster Abstracts Washington, 2010

Washingtom, DC 2010

Item não circula. Consulte sua biblioteca.(Acessar)

4
Array-CGH detection of micro rearrangements in mentally retarded individuals clinical significance of imbalances present both in affected children and normal parents
Array-CGH detection of micro rearrangements in mentally retarded individuals clinical significance of imbalances present both in affected children and normal parents
Material Type:
Artigo 		Adicionar ao Meu Espaço

Array-CGH detection of micro rearrangements in mentally retarded individuals clinical significance of imbalances present both in affected children and normal parents

Carla Rosenberg Jeroen Knijnenburg; E Bakker; Angela M Vianna-Morgante; W Sloos; Paulo A Otto; M Kriek; K Hansson; Ana Cristina Victorino Krepischi; H Fiegler; N. P Carter; E. K Bijlsma; A Van Haeringen; K Szuhai; H. J Tanke

Journal of Medical Genetics v. 43, p. 180-186, 2006

London 2006

Item não circula. Consulte sua biblioteca.(Acessar)

5
Array-CGH detection of micro rearrangements in mentally retarded individuals clinical significance of imbalances present both in affected children and normal parents
Array-CGH detection of micro rearrangements in mentally retarded individuals clinical significance of imbalances present both in affected children and normal parents
Material Type:
Artigo 		Adicionar ao Meu Espaço

Array-CGH detection of micro rearrangements in mentally retarded individuals clinical significance of imbalances present both in affected children and normal parents

C Rosenberg Jeroen Knijnenburg; E Bakker; Angela Maria Vianna-Morgante; W Sloos; Paulo Alberto Otto; M Kriek; K Hansson; Ana Cristina Victorino Krepischi-Santos; H Fiegler; N. P Carter; E. K Bijlsma; A Van Haeringen; K Szuhai; H. J Tanke

Journal of Medical Genetics v. 43, p. 180-186, 2006

London 2006

Item não circula. Consulte sua biblioteca.(Acessar)

6
Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome
Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome

Juliana Forte Mazzeu Ana Cristina Victorino Krepischi; Carla Rosenberg; Karoly Szuhai; Jeroen Knijnenburg; Janneke M. M Weiss; Irina E Kerkis; Zan Mustacchi; Guilherme Colin; Rômulo Mombach; Rita de Cássia M Pavanello; Paulo A Otto; Angela M Vianna-Morgante

American Journal of Medical Genetics. Part A v. 143A, n. 15, p. 1790-1795, 2007

New York 2007

Acesso online

7
Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy
Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy
Material Type:
Artigo 		Adicionar ao Meu Espaço

Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy

Ana Cristina Victorino Krepischi Jeroen Knijnenburg; Debora Romeu Bertola; Chong Ae Kim; Peter Lees Pearson; Emilia Bijlsma; Karoly Szuhai; Fernando Kok; Angela M Vianna-Morgante; Carla Rosenberg

Epilepsia Hoboken v. 51 n. 12, p. 2457-2460, dec. 2010

Hoboken 2010

Item não circula. Consulte sua biblioteca.(Acessar)

8
Insight into the mechanisms and consequences of recurrent telomere capture associated with a sub-telomeric deletion
Insight into the mechanisms and consequences of recurrent telomere capture associated with a sub-telomeric deletion
Material Type:
Artigo 		Adicionar ao Meu Espaço

Insight into the mechanisms and consequences of recurrent telomere capture associated with a sub-telomeric deletion

Alexsandro dos Santos Francine Campagnari; Ana Cristina Victorino Krepischi; Maria de Lourdes Ribeiro Câmara; Rita de Cássia E. de Arruda Brasil; Ligia Vieira; Angela M Vianna-Morgante; Paulo A Otto; Peter L Pearson; Carla Rosenberg

Chromosome Research Dordrecht v. 26, p. 191-198, 2018

Dordrecht 2018

Item não circula. Consulte sua biblioteca.(Acessar)

9
Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome
Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome

Juliana Forte Mazzeu Ana Cristina Victorino Krepischi-Santos; Carla Rosenberg; Karoly Szuhai; Jeroen Knijnenburg; Janneke M. M Weiss; Irina E Kerkis; Zan Mustacchi; Guilherme Colin; Rômulo Mombach; Rita de Cássia M Pavanello; Paulo Alberto Otto; Angela Maria Vianna-Morgante

American Journal of Medical Genetics. Part A v. 143A, n. 15, p. 1790-1795, 2007

New York 2007

Acesso online

10
Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy
Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy
Material Type:
Artigo 		Adicionar ao Meu Espaço

Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy

Ana Cristina Victorino Krepischi Jeroen Knijnenburg; Debora Romeu Bertola; Chong Ae Kim; Peter Lees Pearson; Emilia Bijlsma; Karoly Szuhai; Fernando Kok; Angela Maria Vianna-Morgante; Carla Rosenberg

Epilepsia Hoboken v. 51 n. 12, p. 2457-2460, dec. 2010

Hoboken 2010

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Vianna-Morgante, A
  2. Rosenberg, C
  3. Krepischi, A
  4. Otto, P
  5. Pearson, P

Neste Assunto:

  1. Doenças Genéticas
  2. Genética Médica
  3. Retardo Mental
  4. Genética
  5. Genomas

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

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