Trisomy 22 and intersex.

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.

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Bibliografiske detaljer
Main Authors: Nicholl, R M, Grimsley, L, Butler, L, Palmer, R W, Rees, H C, Savage, M O, Costeloe, K
Format: Artigo
Sprog:Inglês
Udgivet: 1994
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1061073/
https://ncbi.nlm.nih.gov/pubmed/8092876
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