Your browser doesn't support javascript.
loading
Maternal versus paternal inheritance of a 132 bp 11p15.5 microdeletion affecting KCNQ1OT1 and associated phenotypes.
Stoltze, Ulrik Kristoffer; Hansen, Thomas Van Overeem; Brok, Jesper Sune; Grønskov, Karen; Tumer, Zeynep; Ahlborn, Lise Barlebo; Schmiegelow, Kjeld; Wadt, Karin A W.
Afiliación
  • Stoltze UK; Department of Clinical Genetics, Rigshospitalet, Copenhagen, Denmark ulrik.kristoffer.stoltze@regionh.dk.
  • Hansen TVO; Department of Pediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen, Denmark.
  • Brok JS; Department of Clinical Genetics, Rigshospitalet, Copenhagen, Denmark.
  • Grønskov K; Department of Pediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen, Denmark.
  • Tumer Z; Department of Clinical Genetics, Rigshospitalet, Copenhagen, Denmark.
  • Ahlborn LB; Department of Clinical Genetics, Rigshospitalet, Copenhagen, Denmark.
  • Schmiegelow K; Department of Clinical Medicine, Rigshospitalet, Copenhagen, Denmark.
  • Wadt KAW; Center for Genomic Medicine, Rigshospitalet, Copenhagen, Denmark.
J Med Genet ; 60(2): 128-130, 2023 02.
Article en En | MEDLINE | ID: mdl-35772845
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome de Beckwith-Wiedemann / ARN Largo no Codificante / Herencia Materna / Herencia Paterna Tipo de estudio: Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: J Med Genet Año: 2023 Tipo del documento: Article País de afiliación: Dinamarca
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome de Beckwith-Wiedemann / ARN Largo no Codificante / Herencia Materna / Herencia Paterna Tipo de estudio: Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: J Med Genet Año: 2023 Tipo del documento: Article País de afiliación: Dinamarca