Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly
Authors:
- 18 May 1998
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 77 (3) , 188-197
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- Adenomatous polyposis coli and a cytogenetic deletion of chromosome 5 resulting from a maternal intrachromosomal insertion.Journal of Medical Genetics, 1994
- Congenital contractural arachnodactyly in two double second cousins: possible homozygosityClinical Genetics, 1993
- An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations.Journal of Medical Genetics, 1992
- Double chromosome anomaly: Interstitial deletion 5q and reciprocal translocation (1;11) (p22;q21)American Journal of Medical Genetics, 1990
- Deletion of chromosome 5q and familial adenomatous polyposis.Journal of Medical Genetics, 1989
- A severe form of congenital contractural arachnodactyly in two newborn infantsAmerican Journal of Medical Genetics, 1986
- Gardner syndrome in a man with an interstitial deletion of 5qAmerican Journal of Medical Genetics, 1986
- Differential activity of maternally and paternally derived chromosome regions in miceNature, 1985
- A case of an interstitial deletion of the long arm of chromosome 5: 46,XX,del(5)(q15q22)Journal of Human Genetics, 1984
- Interstitial deletion in the long arm of chromosome no. 5Clinical Genetics, 1983