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PMID: 991443 Published · ppublish English Case Reports Journal Article

Structural aberrations of the long arm of chromosome no. 22. Report fo a family with translocation t(11;22) (q25;q11).

Clinical genetics ·Vol. 10 ·No. 6 ·1976-12-00 ·Pages 329-36

Fu W, Borgaonkar DS, Ladewig PP, Weaver J, Pomerance HH

Abstract

A chromosomal translocation t(11;22) (q25q11) is described in a family. Four members, in two generations, had the same translocation but showed phenotypic variation. Case reports of chromosome aberrations involving the long arm of chromosome 22 associated with and without chronic myeloid leukemia (CML) are reviewed. It appears that the distal segment of the long arm or chromosome 22 is either translocated or deleted, resulting in congenital anomalies, presumably due to chromosome imbalance. In other instances, a specific breakpoint on 22q results in the origin of Philadelphia chromosome (Ph1) associated with CML.

MeSH Terms
Abnormalities, Multiple/genetics Child Chromosome Aberrations Chromosomes, Human, 21-22 and Y Chromosomes, Human, 6-12 and X Female Heart Defects, Congenital/genetics Humans Intellectual Disability/genetics Male Pedigree Translocation, Genetic
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Fu W
Borgaonkar D S
Ladewig P P
Weaver J
Pomerance H H
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
1976-12-00
Pages
329-36
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
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