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Refinado por: Nome da Publicação: American Journal of Medical Genetics. Part A remover
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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
Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation
Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation
Material Type:
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Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation

Lucilene Arilho Ribeiro Antonio Richieri-Costa

American Journal of Medical Genetics. Part A v. 136, n. 4, p. 348-349, Aug., 2005

Hoboken 2005

Item não circula. Consulte sua biblioteca.(Acessar)

3
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation
Material Type:
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Single median maxillary central incisor, hypophyseal tumor, and SHH mutation

Lucilene Arilho Ribeiro Antonio Richieri-Costa

American Journal of Medical Genetics. Part A v. 136, n. 4, p. 346-347, Aug., 2005

Hoboken 2005

Item não circula. Consulte sua biblioteca.(Acessar)

4
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation
Material Type:
Artigo 		Adicionar ao Meu Espaço

Single median maxillary central incisor, hypophyseal tumor, and SHH mutation

Lucilene Arilho Ribeiro Antonio Richieri-Costa

American Journal of Medical Genetics. Part A v. 136, n. 4, p. 346-347, Aug., 2005

Hoboken 2005

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
Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation
Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation
Material Type:
Artigo 		Adicionar ao Meu Espaço

Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation

Lucilene Arilho Ribeiro Antonio Richieri-Costa

American Journal of Medical Genetics. Part A v. 136, n. 4, p. 348-349, Aug., 2005

Hoboken 2005

Item não circula. Consulte sua biblioteca.(Acessar)

7
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:
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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)

8
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)

9
AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations
AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations
Material Type:
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AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations

Angeli, Claudia B. ; Capelli, Leonardo P. ; Auricchio, Maria Teresa B.M. ; Vianna-Morgante, Angela M. ; Mingroni-Netto, Regina C. ; Leal-Mesquita, Emygdia R. ; Ribeiro-dos-Santos, Ândrea K.C. ; Ferrari, Iris ; Oliveira, Silviene F. ; Klautau-Guimarães, Maria de Nazaré

American journal of medical genetics, 2005-01, Vol.132A (2), p.210-214 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

Texto completo disponível

Citações Citado por
10
Relationship between polymorphisms in genes involved in homocysteine metabolism and maternal risk for Down syndrome in Brazil
Relationship between polymorphisms in genes involved in homocysteine metabolism and maternal risk for Down syndrome in Brazil
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Relationship between polymorphisms in genes involved in homocysteine metabolism and maternal risk for Down syndrome in Brazil

da Silva, Luciana Rodrigues Jacy ; Vergani, Naja ; Galdieri, Luciano de Camargo ; Ribeiro Porto, Marianna Picarelli ; Longhitano, Silvia Bragagnolo ; Brunoni, Decio ; D'Almeida, Vânia ; Alvarez Perez, Ana Beatriz

American journal of medical genetics. Part A, 2005-06, Vol.135A (3), p.263-267 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

Texto completo disponível

Citações Citado por
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Deste Autor:

  1. Richieri-Costa, A
  2. Ribeiro, L
  3. Bertolacini, C
  4. Giugliani, R
  5. Zechi-Ceide, R

Neste Assunto:

  1. Genetics & Heredity
  2. Life Sciences & Biomedicine
  3. Science & Technology
  4. Humans
  5. Holoprosencefalia

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

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