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PMID: 8808614 Published · ppublish English Letter Research Support, U.S. Gov't, P.H.S.

7q11.23 deletions in Williams syndrome arise as a consequence of unequal meiotic crossover.

American journal of human genetics ·Vol. 59 ·No. 4 ·1996-10-00 ·Pages 958-62

Urbán Z, Helms C, Fekete G, Csiszár K, Bonnet D, Munnich A, Donis-Keller H, Boyd CD

Abstract

暂无摘要

MeSH Terms
Chromosome Mapping Chromosomes, Human, Pair 7 Crossing Over, Genetic Gene Deletion Genotype Haploidy Humans Meiosis Microsatellite Repeats Polymerase Chain Reaction Williams Syndrome/genetics
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Urbán Z
Helms C
Fekete G
Csiszár K
Bonnet D
Munnich A
Donis-Keller H
Boyd C D
References (14)
14 references, click to expand
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Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1996-10-00
Pages
958-62
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1914803
Subset
IM
Grants
NHGRI NIH HHS · HG00469 · United States
NHLBI NIH HHS · HL37438 · United States
External Links
PubMed source PMC Full Text View journal details
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