Gheid Abuharb

Homozygosity mapping identifies a novel GIPC3 mutation causing congenital nonsyndromic hearing loss in a Saudi family

Khushnooda Ramzan, Mohammed Al‐Owain, Rabab Allam et al. · Gene · 2013 · 18 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +13

A recessive form of Marshall syndrome is caused by a mutation in the <i>COL11A1</i> gene: Figure 1

Ola Khalifa, Faiqa Imtiaz, Rabab Allam et al. · Journal of Medical Genetics · 2012 · 16 citations

Marshall syndrome: Further evidence of a distinct phenotypic entity and report of new findings

Osama Khalifa, Faiqa Imtiaz, Khushnooda Ramzan et al. · American Journal of Medical Genetics Part A · 2014 · 16 citations

Saudi Arabia, Genetics, Pathology +16

Use of beta blockers is associated with hearing loss

Bandar Al‐Ghamdi, Dileep Kumar Rohra, Gheid Abuharb et al. · International Journal of Audiology · 2017 · 11 citations