Partial deletion of the short arm of chromosome 3: further delineation of the 3p25 ‐ 3pter syndrome
- 1 August 1986
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 30 (2) , 127-130
- https://doi.org/10.1111/j.1399-0004.1986.tb00581.x
Abstract
A male newborn with partial deletion of the short arm of chromosome 3 is described. The patient shares most of the features with the previously reported cases. In addition, cardiac, skeletal and gastrointestinal anomalies not previously reported are described. These characteristics may help in further delineation of the syndrome.Keywords
This publication has 6 references indexed in Scilit:
- Partial deletion of the short arm of chromosome 3 (3p25 → 3pter) Further delineation of the clinical phenotypeClinical Genetics, 2008
- Deletion of the short arm of chromosome 3: a case report with necropsy findings.Journal of Medical Genetics, 1984
- A second patient with partial deletion of the short arm of chromosome 3: karyotype 46,XY,del(3)(p25).Journal of Medical Genetics, 1982
- Partial deletion of the short arm of chromosome 3European Journal of Pediatrics, 1981
- PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME-3 - REPORT OF A CASE1980
- A Patient With a Partial Deletion of the Short Arm of Chromosome 3American Journal of Diseases of Children, 1978