Deletion 2q: two new cases with karyotypes 46,XY,del(2)(q31q33) and 46,XX,del(2)(q36).
Open Access
- 1 June 1983
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 20 (3), 199-202
- https://doi.org/10.1136/jmg.20.3.199
Abstract
We describe the clinical and cytogenetic findings of two patients with deletions of the long arm of chromosome 2. One has an interstitial deletion identical to that found in a previously reported patient, although they are phenotypically dissimilar. The other patient has a terminal deletion, the first such deletion reported to date.This publication has 5 references indexed in Scilit:
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- Partial deletion of chromosome 2 mimicking a phenotype of trisomy 18: Case report with autopsyHuman Pathology, 1980
- Interstitial deletion of the long arm of chromosome 2 in a polymalformed newborn-karyotype: 46,XX,del(2)(q21;q24)Human Genetics, 1977
- Etude chromosomique et clinique d'une fillette porteuse d'une deletion (2) (q34q36)Human Genetics, 1976
- Autosomal translocation in a mentally retarded male child with 46,XY,t(2q-;13q+) complement. Case report and review.Journal of Medical Genetics, 1971