Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers-Reference-Cited by-同舟云学术

Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers

Published:2004 Issue:2 Volume:130A Page:128-133
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Arens Y.H.J.M.,Engelen J.J.M.,Govaerts L.C.P.,van Ravenswaay C.M.,Loneus W.H.,van Lent-Albrechts J.C.M.,van der Blij-Philipsen M.,Hamers A.J.H.,Schrander-Stumpel C.T.R.M.

Publisher

Wiley

Subject

Genetics(clinical)

Reference52 articles.

1. Adenomatous polyposis coli and a cytogenetic deletion of chromosome 5 resulting from a maternal intrachromosomal insertion.

2. Identification of an Interstitial Deletion in an Adult Female with Schizophrenia, Mental Retardation, and Dysmorphic Features: Further Support for a Putative Schizophrenia-Susceptibility Locus at 5q21-23.1

3. Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly

4. An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations.

5. Interstitial deletion of band q12 of chromosome 5

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