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Expanding the phenotypic spectrum of COLEC10-Related 3MC syndrome: A glimpse into COLEC10-Related 3MC syndrome in the Ashkenazi Jewish population.
Rabin, Rachel; Hirsch, Yoel; Chung, Wendy K; Ekstein, Josef; Levy-Lahad, Ephrat; Zuckerman, Shachar; Mor-Shaked, Hagar; Meiner, Vardiella; Booth, Kevin T; Pappas, John.
Afiliación
  • Rabin R; Department of Pediatrics, NYU Grossman School of Medicine, New York, New York, USA.
  • Hirsch Y; Dor Yeshorim, Committee for Prevention Jewish Genetic Diseases, Brooklyn, New York, USA.
  • Chung WK; Departments of Pediatrics and Medicine, Columbia University, New York, New York, USA.
  • Ekstein J; Dor Yeshorim, Committee for Prevention Jewish Genetic Diseases, Brooklyn, New York, USA.
  • Levy-Lahad E; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
  • Zuckerman S; Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
  • Mor-Shaked H; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
  • Meiner V; Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
  • Booth KT; Department of Genetics, Hadassah Medical Organization, Jerusalem, Israel.
  • Pappas J; Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
Am J Med Genet A ; 188(10): 3110-3117, 2022 10.
Article en En | MEDLINE | ID: mdl-35943032

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Múltiples / Labio Leporino / Fisura del Paladar Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Múltiples / Labio Leporino / Fisura del Paladar Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos