Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis
Year: 2004
Type: article
Study design: Case Report
Source: Annales de Génétique
Authors: N. Bouayed Abdelmoula, M.F. Portnoï, A. Amouri, A. Arladan, M. Chakroun, A. Saad, M. Hchicha, H. Turki, T. Rebai
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2007144364
