skip to main content
Idioma:
Refinado por: autor: Kim, C remover assunto: Mutação Genética remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Cockayne syndrome type A novel mutations in eight typical patients
Cockayne syndrome type A novel mutations in eight typical patients
Material Type:
Artigo 		Adicionar ao Meu Espaço

Cockayne syndrome type A novel mutations in eight typical patients

Debora R. Bertola Henian Cao; Lilian M. J Albano; Fernando Kok; Maria Joaquina Marques-Dias; Chong A Kim; Robert A Hegele

Journal of human genetics Tokyo v.51, n.8, p.701-705, 2006

Tokyo 2006

Localização: FM - Fac. Medicina    (FM BCSEP 155 2006 )(Acessar)

2
Further evidence that the T73I PTPNII gene mutation is associated with a myeloproliferative disorder in noonan syndrome
Further evidence that the T73I PTPNII gene mutation is associated with a myeloproliferative disorder in noonan syndrome
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Further evidence that the T73I PTPNII gene mutation is associated with a myeloproliferative disorder in noonan syndrome

D. R Bertola A. C Pereira; J. D. A Carneiro; C. A Kim; American college of medical genetics (2004 Florida); Annual clinical genetics meeting (Florida 2004)

Resumos Florida, 2004

Florida 2004

Localização: FM - Fac. Medicina    (FM BCSEP 340 2004 )(Acessar)

3
Cockayne syndrome type A novel mutations in eight typical patients
Cockayne syndrome type A novel mutations in eight typical patients
Material Type:
Artigo 		Adicionar ao Meu Espaço

Cockayne syndrome type A novel mutations in eight typical patients

Debora R. Bertola Henian Cao; Lilian M. J Albano; Fernando Kok; Maria Joaquina Marques-Dias; Chong A Kim; Robert A Hegele

Journal of human genetics Tokyo v.51, n.8, p.701-705, 2006

Tokyo 2006

Localização: FM - Fac. Medicina    (FM BCSEP 155 2006 )(Acessar)

4
Richieri-Costa-Pereira syndrome expanding its phenotypicand genotypic spectrum
Richieri-Costa-Pereira syndrome expanding its phenotypicand genotypic spectrum
Material Type:
Artigo 		Adicionar ao Meu Espaço

Richieri-Costa-Pereira syndrome expanding its phenotypicand genotypic spectrum

D R Bertola G Hsia; L Alvizi; A Gardham; E. L Wakeling; G. L Yamamoto; R. S Honjo; L. A. N Oliveira; R. C. Di Francesco; B A Perez; C A Kim; Maria Rita Passos-Bueno

Clinical Genetics Hoboken online, p. 1-12, Feb. 2018

Hoboken 2018

Localização: FM - Fac. Medicina    (OPI 26383 2018 )(Acessar)

Personalize Seus Resultados

  1. Editar

Refine Search Results

Data de Publicação 

De até
Refinar

Novas Pesquisas Sugeridas

Ignorar minha busca e procurar por tudo

Deste Autor:

  1. Bertola, D
  2. Kim, C
  3. Kok, F
  4. Albano, L
  5. Marques-Dias, M

Neste Assunto:

  1. Genótipos
  2. Fenótipos
  3. Doenças Neurodegenerativas
  4. Disostose Crâniofacial
  5. Malformações

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

Buscando em bases de dados remotas. Favor aguardar.