Home LiteratureArticle Details
PMID: 65235 Published · ppublish English Case Reports Journal Article

Non-fluorescent Y chromosome in a male infant with Turner's symptoms and XO/XY mosaicism.

Clinical genetics ·Vol. 11 ·No. 3 ·1977-03-00 ·Pages 235-40

Fonatschi C, Flatz SD, Freymann R

Abstract

A 45, X/46,XY mosaicism was found in a male infant with stigmata of Turner's syndrome but normal male external genitalia. In contrast to the Y chromosome of his father, the Y chromosome of the patient does not display either the characteristic brilliant fluorescence or the typical dark heterochromatin staining of the distal long arm. Furthermore, DNA replication in the abnormal Y chromosome was shown to be premature. Mechanisms leading to the observed abnormalities are discussed.

MeSH Terms
DNA Replication Dermatoglyphics Fluorescence Heterochromatin Humans Infant Infant, Newborn Male Mosaicism Phenotype Sex Chromosomes Staining and Labeling Turner Syndrome/genetics
Chemicals
Heterochromatin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Fonatschi C
Flatz S D
Freymann R
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
1977-03-00
Pages
235-40
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
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