Familial chromosome translocation t(3;18)(p21;p11).
- 1 April 1981
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 18 (2) , 119-123
- https://doi.org/10.1136/jmg.18.2.119
Abstract
A familial translocation t(3;18)(p21;p11) was observed in a newborn male. He had multiple malformations resuting from partial trisomy 3 and partial monosomy 18. The mother, maternal uncle and maternal grandmother were balanced translocation carriers. A daughter of the maternal uncle with similar malformations probably had the same unbalanced karytope as the proband.This publication has 5 references indexed in Scilit:
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- An unusual chromosomal segregation in a family with a translocation between chromosomes 3 and 12Journal of Medical Genetics, 1974
- [Trisomy for the distal part of the short arm of the number 3 chromosome in 3 siblings. First example of chromosomal insertion: INS(7;3)(q 31;p 21 p 26)].1972
- FAMILIAL DE LANGE SYNDROME WITH CHROMOSOME ABNORMALITIESPediatrics, 1966