Home LiteratureArticle Details
PMID: 1240775 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, Non-P.H.S.

X-autosome translocation with a 47,XXXY qs,t(9p-;Xq+) karyotype.

Birth defects original article series ·Vol. 11 ·No. 5 ·1975-00-00 ·Pages 247-53

Dumars KW, Reed P, Lawce HJ

Abstract

A male with a karyotype 47,XXXY qs,t(9p-;Xq+) was ascertained utilizing ASG-banding. The karyotype was repeated because the original diagnosis of Klinefelter syndrome (47,XXY) was inconsistent with many of the stigmata present. It is suggested that many karyotypes completed prior to the advent of banding techniques will be repeated in an attempt to provide more accurate diagnosis, describe more aberrations, and possibly establish new syndromes.

MeSH Terms
Child Chromosome Aberrations Chromosome Disorders Chromosomes, Human, 6-12 and X Humans Karyotyping Klinefelter Syndrome/genetics Male Pedigree Sex Chromosomes Translocation, Genetic
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Dumars K W
Reed P
Lawce H J
Article Info
Journal
Birth defects original article series
Abbr.
Birth Defects Orig Artic Ser
ISSN
0547-6844
Published
1975-00-00
Pages
247-53
Language
English
Region
United States
NLM ID
0003403
Subset
IM
External Links
PubMed source
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com