Home LiteratureArticle Details

PMID: 6134086 Published · ppublish English Letter Research Support, U.S. Gov't, P.H.S.

Parental origin of chromosome 15 deletion in Prader-Willi syndrome.

Lancet (London, England) ·Vol. 1 ·No. 8336 ·1983-06-04 ·Pages 1285-6

Butler MG, Palmer CG

Abstract

暂无摘要

MeSH Terms

Adult Chromosome Deletion Chromosomes, Human, 13-15 Female Humans Male Prader-Willi Syndrome/genetics

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Butler M G

Palmer C G

References (5)

5 references, click to expand

On the structure and polymorphism of the human chromosome no. 15.
Hum Genet. 1980;56(1):115-8 PMID: 6162775
Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome.
Clin Genet. 1982 Dec;22(6):315-20 PMID: 7160103
Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi syndrome.
Am J Dis Child. 1968 May;115(5):588-98 PMID: 5645106
Prader-Willi syndrome. A resumé of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence.
J Pediatr. 1972 Aug;81(2):286-93 PMID: 5042487
Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.
N Engl J Med. 1981 Feb 5;304(6):325-9 PMID: 7442771

Article Info

Journal

Lancet (London, England)

Abbr.

Lancet

ISSN

0140-6736

DOI

Published

1983-06-04

Pages

1285-6

Language

English

Region

England

NLM ID

2985213R

PMCID

PMC5510872

Subset

Grants

NIDDK NIH HHS · P30 DK026657 · United States

NIGMS NIH HHS · T32 GM007464 · United States

NIGMS NIH HHS · 5T32 GM07468 · United States

External Links

Analysis Services