Ring chromosome 3 in a retarded boy
- 1 January 1978
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 42 (3) , 345-348
- https://doi.org/10.1007/bf00291318
Abstract
We present a boy with the karyotype 46,XY,r3 and a phenotype with psychomotor and growth retardation, craniofacial anomalies, syndactyly of the toes, and edema of the feet. The karyotypes and phenotypes of both parents are normal.This publication has 7 references indexed in Scilit:
- A case of partial trisomy 3qJournal of Medical Genetics, 1976
- Familial translocation (3p 15p) with partial trisomy for the upper arm of chromosome 3 in two sibsThe Journal of Pediatrics, 1976
- Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).1975
- Partial monosomy 13 as the result of a balanced translocation 3/13 patHuman Genetics, 1975
- [Partial 13 trisomy by maternal 46, XX, t (3; 13) (p 26; q 21) translocation].1974
- Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.1974
- Human ring chromosomes: a report of five cases.1972