Partial trisomy 15q1
- 1 January 1976
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 33 (1) , 77-83
- https://doi.org/10.1007/bf00447290
Abstract
A supernumerary extra chromosome of maternal origin, precisely described from QM- and C-banding patterns, was studied in a mentally defective boy with a severe convulsive disorder. This case is considered to represent a specific phenotype of trisomy 15q1. The suggestion that in cases of partial trisomy 15q different phenotypes are due to the second chromosome involved in interchange is supported by the observation of a tertiary trisomy in 2 sibs. It resulted from a balanced reciprocal translocation in the mother t(8q+15q-) and caused an unusual malformation syndrome (mental deficiency, cleft lip and palate, funnel chest, hypospadias).This publication has 18 references indexed in Scilit:
- UNUSUAL DERMATOGLYPHIC PATTERNS ASSOCIATED WITH CHROMOSOMAL ABNORMALITIES*Journal of Intellectual Disability Research, 2008
- BANDING IDENTIFICATION OF PARTIAL TRISOMY 15 AND OF 8/21 TRANSLOCATIONJournal of Intellectual Disability Research, 2008
- A G-like trisomy with a major 15 proximal supernumerary component derived from a D/E balanced maternal interchangeThe Journal of Pediatrics, 1975
- The possibility of latent centromeres and a proposed nomenclature system for total chromosome and whole arm translocationsCytogenetic and Genome Research, 1975
- A case of partial trisomy 15Journal of Medical Genetics, 1974
- PARTIAL TRISOMY OF CHROMOSOME 15The Lancet, 1973
- PARTIAL TRISOMY 15The Lancet, 1972
- Translocation 8–22 sans changement de longueur et trisomie partielle 8q: Detection par denaturation ménagéeExperimental Cell Research, 1972
- PARTIAL TRISOMY OF CHROMOSOME 15The Lancet, 1972
- CHROMOSOME ABNORMALITIES IN A MOTHER AND TWO MENTALLY RETARDED CHILDRENThe Lancet, 1962