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Refinado por: Nome da Publicação: American Journal of Medical Genetics remover
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1
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia

Paula Iughetti Luís Garcia Alonso; William Wilcox; Nivaldo Alonso

American Journal of Medical Genetics n. 95, p. 482-491, 2000

New York 2000

Item não circula. Consulte sua biblioteca.(Acessar)

2
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia

Paula Iughetti Luís Garcia Alonso; William Wilcox; Nivaldo Alonso

American Journal of Medical Genetics n. 95, p. 482-491, 2000

New York 2000

Item não circula. Consulte sua biblioteca.(Acessar)

3
Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses
Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses
Material Type:
Artigo 		Adicionar ao Meu Espaço

Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses

Maria Rita Passos-Bueno Andréa L Sertié; Antonio Richieri-Costa; Luís G Alonso; Mayana Zatz; Nivaldo Alonso; Decio Brunoni; Sandra F M Ribeiro

American Journal of Medical Genetics New York v. 78, p. 237-241, 1998

New York 1998

Item não circula. Consulte sua biblioteca.(Acessar)

4
Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses
Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses
Material Type:
Artigo 		Adicionar ao Meu Espaço

Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses

Maria Rita Passos-Bueno Andréa L Sertié; Antonio Richieri-Costa; Luís G Alonso; Mayana Zatz; Nivaldo Alonso; Decio Brunoni; Sandra F M Ribeiro

American Journal of Medical Genetics New York v. 78, p. 237-241, 1998

New York 1998

Item não circula. Consulte sua biblioteca.(Acessar)

5
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia

Iughetti, Paula ; Alonso, Luis Garcia ; Wilcox, William ; Alonso, Nivaldo ; Passos-Bueno, Maria Rita

American journal of medical genetics, 2000-12, Vol.95 (5), p.482-491

New York: John Wiley & Sons, Inc

Texto completo disponível

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6
Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses
Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses
Material Type:
Artigo 		Adicionar ao Meu Espaço

Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses

Passos-Bueno, Maria Rita ; Sertié, Andréa L. ; Richieri-Costa, Antonio ; Alonso, Luís G. ; Zatz, Mayana ; Alonso, Nivaldo ; Brunoni, Décio ; Ribeiro, Sandra F.M.

American journal of medical genetics, 1998-07, Vol.78 (3), p.237-241

New York: John Wiley & Sons, Inc

Texto completo disponível

Citações Citado por
7
Description of a new mutation and characterization ofFGFR1, FGFR2, andFGFR3 mutations among Brazilian patients with syndromic craniosynostoses
Description of a new mutation and characterization ofFGFR1, FGFR2, andFGFR3 mutations among Brazilian patients with syndromic craniosynostoses
Material Type:
Artigo 		Adicionar ao Meu Espaço

Description of a new mutation and characterization ofFGFR1, FGFR2, andFGFR3 mutations among Brazilian patients with syndromic craniosynostoses

Passos-Bueno, Maria Rita ; Serti, Andr a L. ; Richieri-Costa, Antonio ; Alonso, Lu s G. ; Zatz, Mayana ; Alonso, Nivaldo ; Brunoni, D cio ; Ribeiro, Sandra F.M.

American journal of medical genetics, 1998-07, Vol.78 (3), p.237-241

Texto completo disponível

Citações Citado por

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Deste Autor:

  1. Alonso, N
  2. Alonso, L
  3. Ribeiro, S
  4. Passos-Bueno, M
  5. Richieri-Costa, A

Neste Assunto:

  1. Genética Médica
  2. Genetics & Heredity
  3. Life Sciences & Biomedicine
  4. Tropical Medicine
  5. Female

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

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