Items where authors include "Al-Mamari, W"

Article

Al-Amri, AH, Al Saegh, A, Al-Mamari, W et al. (10 more authors) (2019) LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss. European Journal of Medical Genetics, 62 (12). 103592. ISSN 1769-7212

Al-Amri, A, Saegh, AA, Al-Mamari, W et al. (6 more authors) (2016) Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family. American Journal of Medical Genetics Part A, 170 (7). pp. 1826-1831. ISSN 1552-4825