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PMID: 1679180 Published · ppublish English Letter Research Support, Non-U.S. Gov't

Genomic imprinting in an Angelman and Prader-Willi translocation family.

Lancet (London, England) ·Vol. 338 ·No. 8767 ·1991-09-07 ·Pages 638-9

Hultén M, Armstrong S, Challinor P, Gould C, Hardy G, Leedham P, Lee T, McKeown C

Abstract

暂无摘要

MeSH Terms
Child Chromosome Aberrations/genetics Chromosome Deletion Chromosome Disorders Chromosomes, Human, Pair 15 Female Humans Male Pedigree Phenotype Prader-Willi Syndrome/genetics Translocation, Genetic/genetics
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Hultén M
Armstrong S
Challinor P
Gould C
Hardy G
Leedham P
Lee T
McKeown C
Article Info
Journal
Lancet (London, England)
Abbr.
Lancet
ISSN
0140-6736
DOI
10.1016/0140-6736(91)90652-6
Published
1991-09-07
Pages
638-9
Language
English
Region
England
NLM ID
2985213R
Subset
IM
Corrections
CommentIn
PMID: 1682673
External Links
PubMed source DOI: 10.1016/0140-6736(91)90652-6 View journal details
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