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Genotype-phenotype correlations analysis of mutations in the phenylalanine hydroxylase (PAH) gene.
Bercovich, Dani; Elimelech, Arava; Zlotogora, Joel; Korem, Sigal; Yardeni, Tal; Gal, Nurit; Goldstein, Nurit; Vilensky, Bela; Segev, Roni; Avraham, Smadar; Loewenthal, Ron; Schwartz, Gerard; Anikster, Yair.
Afiliação
  • Bercovich D; MIGAL, Galilee Technology Center, Human Molecular Genetics and Pharmacogenetics Laboratory, Kiryat Shmona, Israel. danib@migal.org.il.
  • Elimelech A; Tel-Hai Academic College, Upper Galilee, Israel. danib@migal.org.il.
  • Zlotogora J; MIGAL, Galilee Technology Center, Human Molecular Genetics and Pharmacogenetics Laboratory, Kiryat Shmona, Israel.
  • Korem S; Department of Genetic Community, Public Health Services, Health Ministry and Hebrew University, Jerusalem, Israel.
  • Yardeni T; MIGAL, Galilee Technology Center, Human Molecular Genetics and Pharmacogenetics Laboratory, Kiryat Shmona, Israel.
  • Gal N; Tel-Hai Academic College, Upper Galilee, Israel.
  • Goldstein N; MIGAL, Galilee Technology Center, Human Molecular Genetics and Pharmacogenetics Laboratory, Kiryat Shmona, Israel.
  • Vilensky B; Metabolic Disease Unit, Safra Children's Hospital, Sheba Medical Center, Tel-Hashomer, Israel.
  • Segev R; Metabolic Disease Unit, Safra Children's Hospital, Sheba Medical Center, Tel-Hashomer, Israel.
  • Avraham S; Metabolic Disease Unit, Safra Children's Hospital, Sheba Medical Center, Tel-Hashomer, Israel.
  • Loewenthal R; Metabolic Disease Unit, Safra Children's Hospital, Sheba Medical Center, Tel-Hashomer, Israel.
  • Schwartz G; Metabolic Disease Unit, Safra Children's Hospital, Sheba Medical Center, Tel-Hashomer, Israel.
  • Anikster Y; Tissue Typing Unit and Safra Children Hospital, Sheba Medical Center, Tel-Hashomer, Israel.
J Hum Genet ; 53(5): 407-418, 2008.
Article em En | MEDLINE | ID: mdl-18299955
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Fenilalanina Hidroxilase / Mutação Limite: Humans Idioma: En Ano de publicação: 2008 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Fenilalanina Hidroxilase / Mutação Limite: Humans Idioma: En Ano de publicação: 2008 Tipo de documento: Article