Translocation Y/5 resulting in Cri du Chat syndrome
- 1 December 1977
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 12 (6) , 319-322
- https://doi.org/10.1111/j.1399-0004.1977.tb00949.x
Abstract
A case of 45,X,del(5)(p14/45,X,t(Y;5)(q11;p14) mosaicism is described. The patient displays the clinical features of the Cri du Chat syndrome, together with gross malformation of the distal left arm. The presence of male sex development is consistent with the location of factor(s) controlling the male sex determination in the paracentromeric area of the Y chromosome.This publication has 9 references indexed in Scilit:
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