Novel Mutation in Wolcott–Rallison Syndrome with Variable Expression in Two Omani Siblings

by Siham Al-Sinani, Saif Al-Yaarubi, SW Sharef, Fathyia Al-Murshedi, Watfa Al-Maamari
Published 2015-03-01

Further Clinical and Molecular Delineation of Xp11.22 Deletion Syndrome: A Case Report

by Halima Al-Shehhi, Ahlam Gabr, Intisar Al-Haddabi, Raquel Tena, Anna Baquero, Watfa Al-Maamari, Almundher Al-Maawali
Published 2019-09-01