The problem of partial trisomy 22 reconsidered
- 1 January 1978
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 45 (1), 97-101
- https://doi.org/10.1007/bf00277580
Abstract
A patient with partial trisomy 22 (PT22) is presented. Inheritance is presumed to be due to secondary nondisjunction in her mother, who has a balanced translocation t(11;22)(q25;q13). The problem of the phenotypic heterogeneity observed with this chromosome change is discussed.This publication has 10 references indexed in Scilit:
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- Partial trisomy 22: A recognizable syndromeClinical Genetics, 1977
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- The Problem of Trisomy 22Clinical Pediatrics, 1976
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- PARTIAL TRISOMY FOR LONG ARM OF CHROMOSOME 11 DUE TO T(11 - 22)(Q231 - Q111) TRANSLOCATION1976
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