✦ LIBER ✦

Terminal deletion of Xp22.3 associated with contiguous gene syndrome: L�ri-Weill dyschondrosteosis, developmental delay, and ichthyosis

✍ Scribed by Vassal, Humberto ;Medeira, Ana ;Cordeiro, Isabel ;Santos, Helo�sa G. ;Castedo, S�rgio ;Saraiva, C�lia ;da Silva, Patricia Mendes ;Monteiro, Carolino

Publisher: John Wiley and Sons
Year: 2001
Tongue: English
Weight: 266 KB
Volume: 99
Category: Article
ISSN: 0148-7299
DOI: 10.1002/1096-8628(20010401)99:4<331::aid-ajmg1175>3.0.co;2-w

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Contiguous gene syndrome due to a matern

Contiguous gene syndrome due to a maternally inherited 8.41 Mb distal deletion of chromosome band Xp22.3 in a boy with short stature, ichthyosis, epilepsy, mental retardation, cerebral cortical heterotopias and Dandy–Walker malformation

✍ M.A.M. van Steensel; M. Vreeburg; J. Engelen; S. Ghesquiere; A.P.A. Stegmann; J. 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 159 KB 👁 2 views