skip to main content
Idioma:
Refinado por: autor: Rosenberg, C remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
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)

2
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)

3
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability
Material Type:
Artigo 		Adicionar ao Meu Espaço

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

Charles Shaw-Smith Alan M Pittman; Lionel Willatt; Howard Martin; Lisa Rickman; Susan Gribble; Rebecca Curley; Sally Cumming; Carolyn Dunn; Dimitrios Kalaitzopoulos; Keith R Porter; Elena Prigmore; Ana Cristina Victorino Krepischi; Monica Castro Varela; Celia Priszkulnik Koiffmann; Andrew J Lees; Carla Rosenberg; Helen V Firth; Rohan de Silva; Nigel P Carter

Nature Genetics v. 38, n. 9, p. 1032-1037, sept. 2006

New York 2006

Item não circula. Consulte sua biblioteca.(Acessar)

4
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability
Material Type:
Artigo 		Adicionar ao Meu Espaço

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

Charles Shaw-Smith Alan M Pittman; Lionel Willatt; Howard Martin; Lisa Rickman; Susan Gribble; Rebecca Curley; Sally Cumming; Carolyn Dunn; Dimitrios Kalaitzopoulos; Keith R Porter; Elena Prigmore; Ana Cristina Victorino Krepischi-Santos; Monica Castro Varela; Célia Priszkulnik Koiffmann; Andrew J Lees; Carla Rosenberg; Helen V Firth; Rohan de Silva; Nigel P Carter

Nature Genetics v. 38, n. 9, p. 1032-1037, sept. 2006

New York 2006

Item não circula. Consulte sua biblioteca.(Acessar)

5
Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
Material Type:
Artigo 		Adicionar ao Meu Espaço

Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

David T. Miller Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John, A Crolla; E Eichler; Charles J Epstein; W. Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert H Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter

The American Journal of Human Genetics Cambridge v. 86 n. 5, p. 749-764, may 2010

Cambridge 2010

Item não circula. Consulte sua biblioteca.(Acessar)

6
Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
Material Type:
Artigo 		Adicionar ao Meu Espaço

Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

David T. Miller Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John, A Crolla; E Eichler; Charles J Epstein; W. Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert H Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter

The American Journal of Human Genetics Cambridge v. 86 n. 5, p. 749-764, may 2010

Cambridge 2010

Item não circula. Consulte sua biblioteca.(Acessar)

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Data de Publicação 

De até
Refinar

Novas Pesquisas Sugeridas

Ignorar minha busca e procurar por tudo

Deste Autor:

  1. Carter, N
  2. Rosenberg, C
  3. Gribble, S
  4. Kalaitzopoulos, D
  5. Fiegler, H

Neste Assunto:

  1. Doenças Genéticas
  2. Malformações
  3. Deleção De Genes
  4. Retardo Mental
  5. Diagnóstico Clínico

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

Buscando em bases de dados remotas. Favor aguardar.