Home LiteratureArticle Details
PMID: 4278407 Published · ppublish English Journal Article

Rare translocation 47,XY,t(12;21) in Down's syndrome.

Human heredity ·Vol. 24 ·No. 2 ·1974-00-00 ·Pages 160-6

Mikkelsen M

Abstract

暂无摘要

MeSH Terms
Adolescent Chromosome Aberrations Chromosomes, Human, 21-22 and Y Chromosomes, Human, 6-12 and X Down Syndrome/blood,genetics Female Fluorescence Humans Karyotyping Male Middle Aged Translocation, Genetic
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Mikkelsen M
Article Info
Journal
Human heredity
Abbr.
Hum Hered
ISSN
0001-5652
DOI
10.1159/000152648
Published
1974-00-00
Pages
160-6
Language
English
Region
Switzerland
NLM ID
0200525
Subset
IM
External Links
PubMed source DOI: 10.1159/000152648 View journal details
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

Copyright © 2026.Genelibs Jinan Honghui Biotechnology Co., Ltd. 鲁ICP备20007159号-2