skip to main content
Idioma:
Mostrar Somente
Refinado por: Nome da Publicação: American Journal of Medical Genetics. Part A remover 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
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)

3
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)

4
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)

5
Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes report of four brazilian patients
Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes report of four brazilian patients
Material Type:
Artigo 		Adicionar ao Meu Espaço

Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes report of four brazilian patients

Lucilene Arilho Ribeiro Rodrigo Gonçalves Quiezi; Adriana Nascimento; Claudia Danielli Pereira Bertolacini; Antonio Richieri-Costa

American Journal of Medical Genetics, Part A Hoboken v. 152A, n. 7, p. 1688-1694, July 2010

Hoboken 2010

Item não circula. Consulte sua biblioteca.(Acessar)

6
Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes report of four brazilian patients
Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes report of four brazilian patients
Material Type:
Artigo 		Adicionar ao Meu Espaço

Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes report of four brazilian patients

Lucilene Arilho Ribeiro Rodrigo Gonçalves Quiezi; Adriana Nascimento; Claudia Danielli Pereira Bertolacini; Antonio Richieri-Costa

American Journal of Medical Genetics, Part A Hoboken v. 152A, n. 7, p. 1688-1694, July 2010

Hoboken 2010

Item não circula. Consulte sua biblioteca.(Acessar)

7
Language skills and neuropsychological performance in patients with SHH mutations and holoprosencephaly-like phenotype
Language skills and neuropsychological performance in patients with SHH mutations and holoprosencephaly-like phenotype
Material Type:
Artigo 		Adicionar ao Meu Espaço

Language skills and neuropsychological performance in patients with SHH mutations and holoprosencephaly-like phenotype

Giselda Santiago Dagma Venturini Marques Abramides; Luciana Paula Maximino De Vitto; Lucilene Arilho Ribeiro; Sílvio Garcia Meira Júnior; Antonio Richieri-Costa

American Journal of Medical Genetics. Part A Hoboken v. 104A, n. 19, p. 2085-2090, Oct. 2006

Hoboken 2006

Acesso online

8
Language skills and neuropsychological performance in patients with SHH mutations and holoprosencephaly-like phenotype
Language skills and neuropsychological performance in patients with SHH mutations and holoprosencephaly-like phenotype
Material Type:
Artigo 		Adicionar ao Meu Espaço

Language skills and neuropsychological performance in patients with SHH mutations and holoprosencephaly-like phenotype

Giselda Santiago Dagma Venturini Marques Abramides; Luciana Paula Maximino De Vitto; Lucilene Arilho Ribeiro; Sílvio Garcia Meira Júnior; Antonio Richieri-Costa

American Journal of Medical Genetics. Part A Hoboken v. 104A, n. 19, p. 2085-2090, Oct. 2006

Hoboken 2006

Acesso online

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)

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

Buscando em bases de dados remotas. Favor aguardar.