The dup(17p) syndrome
- 1 March 1982
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 11 (3) , 299-304
- https://doi.org/10.1002/ajmg.1320110306
Abstract
In a 42-month-old girl a duplicated 17p chromosome anomaly was identified by trypsin-Giemsa banding techniques. The clinical findings are compared with those of previous case reports. Common phenotypics changes include failure to thrive; hypoplastic, apparently low-set ears; micrognathia; flexion abnormalities of fingers; and foot abnormalities.Keywords
This publication has 6 references indexed in Scilit:
- Pure trisomy 17p in 60% of cellsHuman Genetics, 1979
- An extra small metacentric chromosome identified as a deleted chromosome No. 17Clinical Genetics, 1976
- An improved technique for selective silver staining of nucleolar organizer regions in human chromosomesHuman Genetics, 1976
- Trisomy of the short arm of chromosome 17Human Genetics, 1974
- A simple technique for demonstrating centromeric heterochromatinExperimental Cell Research, 1972
- A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMESThe Lancet, 1971