A Probable Case of Incomplete Trisomy of a Chromosome of the 13-15 Group
Open Access
- 1 June 1965
- journal article
- Published by BMJ in Journal of Medical Genetics
- Vol. 2 (2), 136-141
- https://doi.org/10.1136/jmg.2.2.136
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- A PARTIAL MONGOLThe Lancet, 1963
- TRISOMY OF CHROMOSOMES 13–15 AND 17–18: ITS ASSOCIATION WITH INFANTILE ARTERIOSCLEROSISThe American Journal of the Medical Sciences, 1962
- An aberrant small acrocentric chromosomeAnnals of Human Genetics, 1962
- Multiple Congenital Anomalies in a Negro Infant with 13–15 TrisomySouthern Medical Journal, 1962
- MENTALLY RETARDED SCHIZOID TWIN GIRLS WITH 47 CHROMOSOMESThe Lancet, 1962
- An Apparently Identical Extra Autosome in two Severely Retarded Sisters with Multiple MalformationsCytogenetic and Genome Research, 1962
- TRISOMY 13-15: A CLINICAL SYNDROMEThe Lancet, 1961
- BENIGN CONGENITAL HYPOTONIA WITH CHROMOSOMAL ANOMALYPediatrics, 1961
- Partial-trisomy syndromesChromosoma, 1961
- CHROMOSOMAL TRISOMY ASSOCIATED WITH THE STURGE-WEBER SYNDROMEThe Lancet, 1960