skip to main content
Idioma:
Resultados 1 2 3 4 5 next page
Mostrar Somente
Refinado por: assunto: Holoprosencefalia remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum new case and imaging review of previous cases
Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum new case and imaging review of previous cases
Material Type:
Artigo 		Adicionar ao Meu Espaço

Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum new case and imaging review of previous cases

Antonio Richieri-Costa Lucilene Arilho Ribeiro

American Journal of Medical Genetics. Part A v. 136, n. 4, p. 352-353, Aug., 2005

Hoboken 2005

Item não circula. Consulte sua biblioteca.(Acessar)

2
Holoprosencephaly-like phenotype clinical and genetic perspectives
Holoprosencephaly-like phenotype clinical and genetic perspectives
Material Type:
Artigo 		Adicionar ao Meu Espaço

Holoprosencephaly-like phenotype clinical and genetic perspectives

Antonio Richieri-Costa Lucilene Arilho Ribeiro

American Journal of Medical Genetics Part A Hoboken v. 140A, n. 23, p. 2587-2593, Dec. 2006

Hoboken 2006

Acesso online

3
Variable phenotypic manifestations of a K44N mutation in the TGIF gene
Variable phenotypic manifestations of a K44N mutation in the TGIF gene
Material Type:
Artigo 		Adicionar ao Meu Espaço

Variable phenotypic manifestations of a K44N mutation in the TGIF gene

Antonio Richieri-Costa Lucilene Arilho Ribeiro

Brain & Development Amsterdam v. 30, n. 3, p. 203-205, Mar. 2008

Amsterdam 2008

Acesso online

4
Holoprosencephaly and holoprosencephaly-like phenotypes review of facial and molecular findings in patients from a craniofacial hospital in Brazil
Holoprosencephaly and holoprosencephaly-like phenotypes review of facial and molecular findings in patients from a craniofacial hospital in Brazil
Material Type:
Artigo 		Adicionar ao Meu Espaço

Holoprosencephaly and holoprosencephaly-like phenotypes review of facial and molecular findings in patients from a craniofacial hospital in Brazil

Antonio Richieri-Costa Lucilene Arilho Ribeiro

American Journal of Medical Genetics, Part C, Seminars in Medical Genetics Hoboken v. 154C, n. 1, p. 149-157, Feb. 2010

Hoboken 2010

Item não circula. Consulte sua biblioteca.(Acessar)

5
Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum new case and imaging review of previous cases
Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum new case and imaging review of previous cases
Material Type:
Artigo 		Adicionar ao Meu Espaço

Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum new case and imaging review of previous cases

Antonio Richieri-Costa Lucilene Arilho Ribeiro

American Journal of Medical Genetics. Part A v. 136, n. 4, p. 352-353, Aug., 2005

Hoboken 2005

Item não circula. Consulte sua biblioteca.(Acessar)

6
Holoprosencephaly and holoprosencephaly-like phenotypes review of facial and molecular findings in patients from a craniofacial hospital in Brazil
Holoprosencephaly and holoprosencephaly-like phenotypes review of facial and molecular findings in patients from a craniofacial hospital in Brazil
Material Type:
Artigo 		Adicionar ao Meu Espaço

Holoprosencephaly and holoprosencephaly-like phenotypes review of facial and molecular findings in patients from a craniofacial hospital in Brazil

Antonio Richieri-Costa Lucilene Arilho Ribeiro

American Journal of Medical Genetics, Part C, Seminars in Medical Genetics Hoboken v. 154C, n. 1, p. 149-157, Feb. 2010

Hoboken 2010

Item não circula. Consulte sua biblioteca.(Acessar)

7
Variable phenotypic manifestations of a K44N mutation in the TGIF gene
Variable phenotypic manifestations of a K44N mutation in the TGIF gene
Material Type:
Artigo 		Adicionar ao Meu Espaço

Variable phenotypic manifestations of a K44N mutation in the TGIF gene

Antonio Richieri-Costa Lucilene Arilho Ribeiro

Brain & Development Amsterdam v. 30, n. 3, p. 203-205, Mar. 2008

Amsterdam 2008

Acesso online

8
Holoprosencephaly-like phenotype clinical and genetic perspectives
Holoprosencephaly-like phenotype clinical and genetic perspectives
Material Type:
Artigo 		Adicionar ao Meu Espaço

Holoprosencephaly-like phenotype clinical and genetic perspectives

Antonio Richieri-Costa Lucilene Arilho Ribeiro

American Journal of Medical Genetics Part A Hoboken v. 140A, n. 23, p. 2587-2593, Dec. 2006

Hoboken 2006

Acesso online

9
Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects
Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects
Material Type:
Artigo 		Adicionar ao Meu Espaço

Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects

Lucilene Arilho Ribeiro Rita de Cássia Mecca Guerini; Antonio Richieri-Costa

American Journal of Medical Genetics. Part A v. 136, n. 4, p. 350-351, Aug., 2005

Hoboken 2005

Item não circula. Consulte sua biblioteca.(Acessar)

10
PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI
PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI
Material Type:
Artigo 		Adicionar ao Meu Espaço

PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI

Lucilene Arilho Ribeiro Jeffrey C Murray; Antonio Richieri-Costa

American Journal of Medical Genetics Part A Hoboken v. 140A, n. 23, p. 2584-2586, Dec. 2006

Hoboken 2006

Acesso online

Resultados 1 2 3 4 5 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (12)
  2. Disponível na Biblioteca (2)

Refinar Meus Resultados

Tipo de Recurso 

  1. Artigos  (39)
  2. Produções Acadêmicas  (2)
  3. Mais opções open sub menu

Data de Publicação 

De até
Refinar
  1. Antes de2007  (16)
  2. 2007Até2008  (3)
  3. 2009Até2010  (9)
  4. 2011Até2013  (8)
  5. Após 2013  (5)
  6. Mais opções open sub menu

Novas Pesquisas Sugeridas

Ignorar minha busca e procurar por tudo

Deste Autor:

  1. Richieri-Costa, A
  2. Ribeiro, L
  3. Bicudo, L
  4. Bertolacini, C
  5. Muenke, M

Neste Assunto:

  1. Holoprosencefalia
  2. Mutação Genética
  3. Anormalidades Múltiplas
  4. Fenótipos
  5. Fissura Lábiopalatina

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

Buscando em bases de dados remotas. Favor aguardar.