Trisomy 22 and intersex.
Open Access
- 1 July 1994
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood: Fetal & Neonatal
- Vol. 71 (1) , F57-F58
- https://doi.org/10.1136/fn.71.1.f57
Abstract
Complete trisomy 22, with or without mosaicism, has been reported as a distinct syndrome. In this report an infant is described who was externally male but with female rudimentary internal organs and whose karyotype was 47,XX+22.Keywords
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