Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis

✍ Scribed by N. Bouayed Abdelmoula; M.F. Portnoï; A. Amouri; A. Arladan; M. Chakroun; A. Saad; M. Hchicha; H. Turki; T. Rebai

• Book ID: 113455314
• Publisher: Elsevier Science
• Year: 2004
• Tongue: English
• Weight: 322 KB
• Volume: 47
• Category: Article
• ISSN: 0003-3995
• DOI: 10.1016/j.anngen.2004.03.008