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Bardet Biedl syndrome in South Africa: A single founder mutation.
Fieggen, K; Milligan, C; Henderson, B; Esterhuizen, A I.
Affiliation
  • Fieggen K; Division of Human Genetics, Department of Medicine, University of Cape Town, South Africa. karen.fieggen@uct.ac.za.
S Afr Med J ; 106(6 Suppl 1): S72-4, 2016 May 25.
Article in En | MEDLINE | ID: mdl-27245532
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Testing / Founder Effect / Bardet-Biedl Syndrome / Group II Chaperonins Type of study: Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: S Afr Med J Year: 2016 Document type: Article Affiliation country: South Africa Country of publication: South Africa
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Testing / Founder Effect / Bardet-Biedl Syndrome / Group II Chaperonins Type of study: Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: S Afr Med J Year: 2016 Document type: Article Affiliation country: South Africa Country of publication: South Africa