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Phenotypic heterogeneity in Woodhouse-Sakati syndrome: two new families with a mutation in the C2orf37 gene.
Ben-Omran, Tawfeg; Ali, Rehab; Almureikhi, Mariam; Alameer, Seham; Al-Saffar, Muna; Walsh, Christopher A; Felie, Jillian M; Teebi, Ahmad.
Affiliation
  • Ben-Omran T; Section of Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar. tawben11@hotmail.com
Am J Med Genet A ; 155A(11): 2647-53, 2011 Nov.
Article in En | MEDLINE | ID: mdl-21964978
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arrhythmias, Cardiac / Nuclear Proteins / Diabetes Mellitus / Alopecia / Hypogonadism / Intellectual Disability Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2011 Document type: Article Affiliation country: Qatar Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arrhythmias, Cardiac / Nuclear Proteins / Diabetes Mellitus / Alopecia / Hypogonadism / Intellectual Disability Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2011 Document type: Article Affiliation country: Qatar Country of publication: United States