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Mapping of a novel type III variant of Knobloch syndrome (KNO3) to chromosome 17q11.2.
Khaliq, Shagufta; Abid, Aiysha; White, Dominick R A; Johnson, Colin A; Ismail, Muhammad; Khan, Ayesha; Ayub, Qasim; Sultana, Salma; Maher, Eamonn R; Mehdi, Syed Qasim.
Affiliation
  • Khaliq S; Biomedical and Genetic Engineering Division, Dr. A. Q. Khan Research Laboratories, Islamabad, Pakistan.
Am J Med Genet A ; 143A(23): 2768-74, 2007 Dec 01.
Article in En | MEDLINE | ID: mdl-17975799
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Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 17 Type of study: Prognostic_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2007 Document type: Article Affiliation country: Pakistan Country of publication: United States
Search on Google
Add to My VHL
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 17 Type of study: Prognostic_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2007 Document type: Article Affiliation country: Pakistan Country of publication: United States