Your browser doesn't support javascript.
loading
Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families.
Issa, Yasmin A; Kamal, Lara; Rayyan, Amal Abu; Dweik, Dima; Pierce, Sarah; Lee, Ming K; King, Mary-Claire; Walsh, Tom; Kanaan, Moien.
Affiliation
  • Issa YA; Hereditary Research Laboratory, Bethlehem University, Bethlehem, Palestine.
  • Kamal L; Hereditary Research Laboratory, Bethlehem University, Bethlehem, Palestine.
  • Rayyan AA; Hereditary Research Laboratory, Bethlehem University, Bethlehem, Palestine.
  • Dweik D; Hereditary Research Laboratory, Bethlehem University, Bethlehem, Palestine.
  • Pierce S; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, USA.
  • Lee MK; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, USA.
  • King MC; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, USA.
  • Walsh T; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, USA.
  • Kanaan M; Hereditary Research Laboratory, Bethlehem University, Bethlehem, Palestine.
Eur J Hum Genet ; 24(10): 1430-5, 2016 10.
Article in En | MEDLINE | ID: mdl-27049303
Subject(s)
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ectodermal Dysplasia / Wnt Signaling Pathway / Anodontia / Membrane Proteins / Mutation Type of study: Diagnostic_studies Limits: Adolescent / Child / Female / Humans / Male Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2016 Type: Article
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ectodermal Dysplasia / Wnt Signaling Pathway / Anodontia / Membrane Proteins / Mutation Type of study: Diagnostic_studies Limits: Adolescent / Child / Female / Humans / Male Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2016 Type: Article