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[FROM GENETICS OF FRAGILE X SYNDROME TO DEVELOPMENT OF TARGETED AND PERSONALIZED DRUG THERAPY].
Gabis, Lidia V; Shefer, Shahar; Gruber, Noah; Raviv, Ravit; Cohen, Yoram; Berkenstadt, Michal; Ries-Levavi, Liat; Pinhas-Hamiel, Orit; Elizur, Shai.
Afiliação
  • Gabis LV; The Child Development Center, Sheba Medical Center, Tel Hashomer.
  • Shefer S; Sackler Faculty of Medicine, Tel Aviv University.
  • Gruber N; The Child Development Center, Sheba Medical Center, Tel Hashomer.
  • Raviv R; Unit of Endocrinology and Diabetes, Sheba Medical Center, Tel Hashomer.
  • Cohen Y; Sackler Faculty of Medicine, Tel Aviv University.
  • Berkenstadt M; The Child Development Center, Sheba Medical Center, Tel Hashomer.
  • Ries-Levavi L; IVF Unit, Sheba Medical Center, Tel Hashomer.
  • Pinhas-Hamiel O; Sackler Faculty of Medicine, Tel Aviv University.
  • Elizur S; The Genetic Institute, Sheba Medical Center, Tel Hashomer.
Harefuah ; 157(8): 529-533, 2018 Aug.
Article em He | MEDLINE | ID: mdl-30175572
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Bases de dados: MEDLINE Assunto principal: Testes Genéticos / Medicina de Precisão / Transtorno do Espectro Autista / Síndrome do Cromossomo X Frágil Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child / Female / Humans Idioma: He Revista: Harefuah Ano de publicação: 2018 Tipo de documento: Article
Buscar no Google
Adicionar na Minha BVS
Imprimir
XML
PubMed Links

Bases de dados: MEDLINE Assunto principal: Testes Genéticos / Medicina de Precisão / Transtorno do Espectro Autista / Síndrome do Cromossomo X Frágil Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child / Female / Humans Idioma: He Revista: Harefuah Ano de publicação: 2018 Tipo de documento: Article