Showing results (71-80 of 339) with videos related to

Sort By:
Pageof 34
Human Genetics|March 3, 2007
A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosisGhazanfar Ali, Muhammad Salman Chishti, Syed Irfan Raza, et al.
Molecular Genetics & Genomic Medicine|August 8, 2019
Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohortAmjad Khan, Shirui Han, Rongrong Wang, et al.
Ophthalmic Genetics|January 14, 2017
A novel homozygous variant in the SMOC1 gene underlying Waardenburg anophthalmia syndromeAsmat Ullah, Muhammad Umair, Farooq Ahmad, et al.
Clinical and Experimental Pharmacology & Physiology|November 21, 2019
Upcoming diagnostic biomarkers with promising prospects in neurological disordersWasim Ahmad, Abuzer Ali, Amena Ali, et al.
Journal of Neurosciences in Rural Practice|June 13, 2022
Understanding of Behavioral Problems Among Young Persons with Intellectual Disability: A Self-ReportWasim Ahmad, Priti Arun, Nazli Nazli, et al.
Annals of Human Genetics|February 13, 2018
A novel homozygous missense variant in NECTIN4 (PVRL4) causing ectodermal dysplasia cutaneous syndactyly syndromeFarooq Ahmad, Abdul Nasir, Holger Thiele, et al.
BMC Medical Genetics|June 14, 2012
Novel mutations in natriuretic peptide receptor-2 gene underlie acromesomelic dysplasia, type maroteauxSaadullah Khan, Raja Hussain Ali, Sanaullah Abbasi, et al.
Genetic Testing and Molecular Biomarkers|March 29, 2020
A Novel Missense Variant in the <i>ALX4</i> Gene Underlies Mild to Severe Frontonasal Dysplasia in a Consanguineous FamilyShabir Hussain, Umm-E-Kalsoom, Irfan Ullah, et al.
Pageof 34