On the parental origin of the deletion in Angelman syndrome.

Human genetics ·Vol. 83 ·No. 2 ·1989-09-00 ·Pages 205-7

Knoll JH, Nicholls RD, Lalande M

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/genetics Chromosome Deletion Chromosomes, Human, Pair 15 Female Humans Male Parents Pedigree Syndrome

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Knoll J H

Nicholls R D

Lalande M

References (6)

6 references, click to expand

Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes.
Hum Genet. 1988 Dec;80(4):322-8 PMID: 3198109
Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene cluster.
EMBO J. 1986 Aug;5(8):1857-63 PMID: 3019666
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.
Am J Med Genet. 1989 Feb;32(2):285-90 PMID: 2564739
Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome.
Am J Med Genet. 1989 May;33(1):66-77 PMID: 2568752
Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance.
Am J Med Genet. 1987 Sep;28(1):45-53 PMID: 3674117
Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometry.
Am J Med Genet. 1989 Apr;32(4):545-9 PMID: 2774001

Article Info

Journal

Human genetics

Abbr.

Hum Genet

ISSN

0340-6717

DOI

Published

1989-09-00

Pages

205-7

Language

English

Region

Germany

NLM ID

7613873

Subset

Corrections

CommentOn

PMID: 3198109

External Links

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