| Literature DB >> 8500796 |
C M Tuck-Muller1, J E Martinez, D A Batista, W G Kearns, W Wertelecki.
Abstract
An 11-year-old girl with short stature, mental retardation, and mild dysmorphic features was found to have an inverted duplication of most of the short arm of the X chromosome [dic inv dup(X)(qter-->p22.3::p22.3-->cen:)]. Her mother, who is also short and retarded, carries the same duplication. Fluorescence in situ hybridization with an X chromosome library, and with X centromere-specific alpha satellite and telomere probes, was useful in characterizing the duplication. In most females with structurally abnormal X chromosomes, the abnormal chromosome is inactivated. Although the duplicated X was consistently late replicating in the mother, X chromosome inactivation studies in the proband indicated that in 11% of her lymphocytes the duplicated X was active.Entities:
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Year: 1993 PMID: 8500796 DOI: 10.1007/BF00217366
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132