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1
Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients
Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients

C. Varela Fernando Kok; Nuvarte Setian; C A Kim; Célia Priszkulnik Koiffmann; Annual Meeting of the American Society of Human Genetics (54. 2004 Toronto, Canadá)

Abstracts Toronto, 2004

Toronto 2004

Item não circula. Consulte sua biblioteca.(Acessar)

2
Genetic and molecular analysis of a large cohort of patients with syndromic and non-syndromic trigonocephaly screening for loss of heterozigosity in 9p and 11q regions
Genetic and molecular analysis of a large cohort of patients with syndromic and non-syndromic trigonocephaly screening for loss of heterozigosity in 9p and 11q regions
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Genetic and molecular analysis of a large cohort of patients with syndromic and non-syndromic trigonocephaly screening for loss of heterozigosity in 9p and 11q regions

Fernanda Sarquis Jehee D Johnson; Kikue Terada Abe; L Alonso; N Alonso; C Kim; D Cavalcante; S. A Wall; S Boyd; E Jabs; A. O Wikie; Maria Rita Passos-Bueno; Annual Meeting of the American Society of Human Genetics (54. 2004 Toronto)

Abstracts Toronto, 2004

Toronto 2004

Item não circula. Consulte sua biblioteca.(Acessar)

3
Möbius sequence clinical and pathogenic analysis of 68 patients
Möbius sequence clinical and pathogenic analysis of 68 patients
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Möbius sequence clinical and pathogenic analysis of 68 patients

Maria Joaquina Marques-Dias J. A Paz; Débora R Bertola; Lilian Maria José Albano; M. B Moreira; Claudette Hajaj Gonzalez; Evelyn Kuczynski; M Valente; C. A Kim; Annual Meeting of the American Society of Human Genetics (54. 2004 Toronto)

Abstracts Toronto, 2004

Toronto 2004

Item não circula. Consulte sua biblioteca.(Acessar)

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