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PMID: 1338761 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeat.

Human molecular genetics ·Vol. 1 ·No. 6 ·1992-09-00 ·Pages 451

Crow SR, Harley HG, Brook JD, Rundle SA, Shaw DJ

Abstract

暂无摘要

MeSH Terms
Base Sequence Chromosome Banding Chromosome Mapping Chromosomes, Human, Pair 19 DNA Transposable Elements Humans Myotonic Dystrophy/genetics Polymorphism, Genetic Repetitive Sequences, Nucleic Acid Sequence Deletion
Chemicals
DNA Transposable Elements
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Crow S R
Institute of Medical Genetics, University of Wales College of Medicine, Heath Park, Cardiff, UK.
Harley H G
Brook J D
Rundle S A
Shaw D J
Article Info
Journal
Human molecular genetics
Abbr.
Hum Mol Genet
ISSN
0964-6906
DOI
10.1093/hmg/1.6.451
Published
1992-09-00
Pages
451
Language
English
Region
England
NLM ID
9208958
Subset
IM
External Links
PubMed source DOI: 10.1093/hmg/1.6.451 View journal details
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