Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5
- 1 October 1992
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 44 (3) , 356-360
- https://doi.org/10.1002/ajmg.1320440317
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- Selective linkage disruption in human-Chinese hamster cell hybrids: deletion mapping of the leuS, hexB, emtB, and chr genes on human chromosome 5.Molecular and Cellular Biology, 1982
- Cytologic observations in 35 individuals with a 5p- karyotypeHuman Genetics, 1978
- The cri du chat syndromeHuman Genetics, 1978