Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome

46,XX subjects carrying the testis determining SRY gene usually have a completely male phenotype. In this study, five very rare cases of SRY carrying subjects (two XX males and three XX true hermaphrodites) with various degrees of incomplete masculinisation were analysed in order to elucidate the ca...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Kusz, K., Kotecki, M., Wojda, A., Szarras-Czapnik, M., Latos-Bielenska, A., Warenik-Szymankie..., A., Ruszczynska-Wolsk..., A., Jaruzelska, J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BMJ Group 1999
Aiheet:
Original Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734388/
https://ncbi.nlm.nih.gov/pubmed/10874632
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia