Confirmation of trisomy 22 by trypsin-giemsa staining.
- 1 December 1976
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 13 (6), 517-520
- https://doi.org/10.1136/jmg.13.6.517
Abstract
A small-for-date male infant with mental retardation, microcephaly, malformed ears, preauricular sinuses, epicanthal folds, micrognathia, congenital heart disease, micropenis and micropolygyria of the parietal and occipital lobes of the cerebral cortex was shown to have a 47,XX,+22 karyotype by trypsin-Giemsa banding.This publication has 11 references indexed in Scilit:
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