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Ophthalmic Genetics|February 11, 2011
Molecular characterization of newborn glaucoma including a distinct aniridic phenotypeArif O Khan, Mohammed A Aldahmesh, Lama Al-Abdi, et al.Journal of Medical Genetics|August 25, 2011
Identification of ADAMTS18 as a gene mutated in Knobloch syndromeMohammed A Aldahmesh, Arif O Khan, Jawahir Y Mohamed, et al.Human Genetics|March 21, 2018
Congenital glaucoma and CYP1B1: an old story revisitedHessa S Alsaif, Arif O Khan, Nisha Patel, et al.Ophthalmic Genetics|October 27, 2009
Characterization of CTNS mutations in Arab patients with cystinosisMohammed A Aldahmesh, Amal Humeidan, Hamad A Almojalli, et al.Genes|September 27, 2025
Detection of Chromosomal Aneuploidy Using Exome SequencingMohamed H Al-Hamed, Sateesh Maddirevula, Nabil Moghrabi, et al.American Journal of Human Genetics|November 22, 2011
Recessive mutations in ELOVL4 cause ichthyosis, intellectual disability, and spastic quadriplegiaMohammed A Aldahmesh, Jawahir Y Mohamed, Hisham S Alkuraya, et al.Human Mutation|October 24, 2012
Autozygosity mapping with exome sequence dataIan M Carr, Sanjeev Bhaskar, James O'Sullivan, et al.Nature Protocols|October 30, 2010
MeltMADGE for mutation scanning of specific genes in population studiesKhalid K Alharbi, Mohammed A Aldahmesh, Tom R Gaunt, et al.The British Journal of Ophthalmology|February 10, 2012
RP1 and retinitis pigmentosa: report of novel mutations and insight into mutational mechanismMay Al-Rashed, Leen Abu Safieh, Hisham Alkuraya, et al.Journal of Medical Genetics|April 27, 2013
Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismusAnas M Alazami, Hadia Hijazi, Mohammed S Al-Dosari, et al.Pageof 6