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Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects.
Bolkier, Yoav; Barel, Ortal; Marek-Yagel, Dina; Atias-Varon, Danit; Kagan, Maayan; Vardi, Amir; Mishali, David; Katz, Uriel; Salem, Yishay; Tirosh-Wagner, Tal; Jacobson, Jeffrey M; Raas-Rothschild, Annick; Chorin, Odelia; Eliyahu, Aviva; Sarouf, Yarden; Shlomovitz, Omer; Veber, Alvit; Shalva, Nechama; Javasky, Elisheva; Ben Moshe, Yishay; Staretz-Chacham, Orna; Rechavi, Gideon; Mane, Shrikant; Anikster, Yair; Vivante, Asaf; Pode-Shakked, Ben.
Afiliação
  • Bolkier Y; Pediatric Heart Institute, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Barel O; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Marek-Yagel D; Metabolic Disease Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Atias-Varon D; Genomic Unit, Sheba Cancer Research Center, Sheba Medical Center, Tel Hashomer, Israel.
  • Kagan M; The Wohl Institute for Translational Medicine, Sheba Medical Center, Tel Hashomer, Israel.
  • Vardi A; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Mishali D; Metabolic Disease Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Katz U; Pediatric Nephrology Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Salem Y; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Tirosh-Wagner T; Pediatric Nephrology Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Jacobson JM; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Raas-Rothschild A; Department of Pediatric Cardiac Intensive Care, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Chorin O; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Eliyahu A; Department of Pediatric Cardiac Intensive Care, Edmond Safra International Congenital Heart Center, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Sarouf Y; Pediatric Heart Institute, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Shlomovitz O; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Veber A; Pediatric Heart Institute, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Shalva N; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Javasky E; Pediatric Heart Institute, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Ben Moshe Y; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Staretz-Chacham O; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Rechavi G; Pediatric Imaging Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Mane S; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Anikster Y; The Institute of Rare Diseases, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Vivante A; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Pode-Shakked B; The Institute of Rare Diseases, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
J Med Genet ; 59(7): 691-696, 2022 07.
Article em En | MEDLINE | ID: mdl-34215651
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Heterotaxia / Cardiopatias Congênitas Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Med Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Israel
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Heterotaxia / Cardiopatias Congênitas Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Med Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Israel