Supernumerary chromosome 6 marker associated with paternal uniparental isodisomy of chromosome 6 in a patient with a syndromic disorder of insulin secretion
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference16 articles.
1. Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes;Callen;Am. J. Med. Genet.,1992
2. FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases;Crolla;Am. J. Med. Genet.,1998
3. Diagnostic testing for uniparental disomy: a points to consider statement from the American College of Medical Genetics and Genomics (ACMG);Del Gaudio;Genet. Med.,2020
4. Supernumerary marker chromosomes derived from chromosome 6: cytogenetic, molecular cytogenetic, and array CGH characterization;Huang;Am. J. Med. Genet.,2012
5. Aneurysmal bone cysts and pathologic fracture associated with supernumerary ring chromosome 6 in two unrelated patients;Hurd;Am. J. Med. Genet.,2017
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