Chromosome 1q Terminal Deletion and Congenital Glaucoma: A Case Report

por AlSaad, Rakan, ElMansoury, Jeylan, AlHazzaa, Selwa A.F., Dirar, Qais S.
Publicado 2020

Effect of Pegylated Interferon and Mitomycin C on Ocular Surface Squamous Neoplasia in Xeroderma Pigmentosum: A Case Series

por Dirar, Qais S., Musalem, Hebah M., Al-Hazzaa, Selwa A.F., Al Zoba, Abdulaziz A., Almalki, Amal A.
Publicado 2020

Unusual Association of Aniridia with Aicardi-Goutières Syndrome-Related Congenital Glaucoma in a Tertiary Care Center

por Musalem, Hebah M., Dirar, Qais S., Al-Hazzaa, Selwa A.F., Al Zoba, Abdul-Aziz A., El-Mansoury, Jeylan
Publicado 2018

Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss

por Ramzan, Khushnooda, Al-Numair, Nouf S., Al-Ageel, Sarah, Elbaik, Lina, Sakati, Nadia, Al-Hazzaa, Selwa A. F., Al-Owain, Mohammed, Imtiaz, Faiqa
Publicado 2020

Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes

por Abu-Safieh, Leen, Alrashed, May, Anazi, Shamsa, Alkuraya, Hisham, Khan, Arif O., Al-Owain, Mohammed, Al-Zahrani, Jawahir, Al-Abdi, Lama, Hashem, Mais, Al-Tarimi, Salwa, Sebai, Mohammed-Adeeb, Shamia, Ahmed, Ray-zack, Mohamed D., Nassan, Malik, Al-Hassnan, Zuhair N., Rahbeeni, Zuhair, Waheeb, Saad, Alkharashi, Abdullah, Abboud, Emad, Al-Hazzaa, Selwa A.F., Alkuraya, Fowzan S.
Publicado 2013