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PMID: 6499272 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Abnormal chromosome in Prader-Willi syndrome.

Clinical genetics ·Vol. 26 ·No. 6 ·1984-12-00 ·Pages 597-601

Goh K, Herrmann MA, Campbell RG, Thompson D

Abstract

A Prader-Willi Syndrome (PWS) patient was found to have an extra satellite chromosome, smaller than the normal Chromosome 22, in 60% of her metaphases. G- and C-bandings showed that the extra chromosome did not derive from a Chromosome 15 as has been reported in some PWS patients. Because of variation in chromosomal abnormalities in the PWS patients reported, it was concluded that the chromosomal abnormalities found in them may be a secondary phenomenon rather than the cause of PWS.

MeSH Terms
Adult Chromosome Aberrations Chromosome Banding Chromosome Disorders Chromosomes, Human, 13-15 Chromosomes, Human, 21-22 and Y Female Humans Karyotyping Prader-Willi Syndrome/genetics
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Goh K
Herrmann M A
Campbell R G
Thompson D
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
1984-12-00
Pages
597-601
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
Grants
NIADDK NIH HHS · AM 20494 · United States
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