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Refinado por: Nome da Publicação: American Journal of Medical Genetics. Part A remover assunto: Anormalidades Múltiplas remover
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1
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)

2
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)

3
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)

4
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)

5
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)

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:
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)

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
Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes
Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes
Material Type:
Artigo 		Adicionar ao Meu Espaço

Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes

Roseli Maria Zechi-Ceide Lucilene Arilho Ribeiro; Salmo Raskin; Claudia Danielli Pereira Bertolacini; Maria Leine Guion-Almeida; Antonio Richieri-Costa

American Journal of Medical Genetics. Part A Hoboken v. 149A, n. 6, p. 1277-1279, June 2009

Hoboken 2009

Item não circula. Consulte sua biblioteca.(Acessar)

10
Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes
Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes
Material Type:
Artigo 		Adicionar ao Meu Espaço

Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes

Roseli Maria Zechi-Ceide Lucilene Arilho Ribeiro; Salmo Raskin; Claudia Danielli Pereira Bertolacini; Maria Leine Guion-Almeida; Antonio Richieri-Costa

American Journal of Medical Genetics. Part A Hoboken v. 149A, n. 6, p. 1277-1279, June 2009

Hoboken 2009

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Richieri-Costa, A
  2. Ribeiro, L
  3. Raskin, S
  4. Guion-Almeida, M
  5. Guerini, R

Neste Assunto:

  1. Holoprosencefalia
  2. Maxila
  3. Desenvolvimento Físico
  4. Fissura Lábiopalatina Bilateral
  5. Genes

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

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