A case of double trisomy in a liveborn infant: 48, XXY, + 13
- 1 February 1977
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 11 (2), 147-150
- https://doi.org/10.1111/j.1399-0004.1977.tb01292.x
Abstract
Ambiguous genitalia, microcephaly, microphthalmia, hypotelorism, single choanal opening, low-set ears, simian creases, Tetralogy of Fallot, bilateral hydronephrosis and absence of the left ureter characterized an infant that died 1 h postpartum with the karyotype 48,XXY,+13.This publication has 2 references indexed in Scilit:
- A double aneuploid mosaic: trisomy 13 and XXY.Journal of Medical Genetics, 1972
- A NEW DOUBLE ANEUPLOID: XXY D-TRISOMYThe Lancet, 1965