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BMC Medical Genetics|July 22, 2018
Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairmentIsabelle Schrauwen, Imen Chakchouk, Anushree Acharya, et al.Clinical and Experimental Dermatology|February 12, 2022
Exome sequencing reveals the first intragenic deletion in ABCA5 underlying autosomal recessive hypertrichosisRubab Raza, Asmat Ullah, Nighat Haider, et al.Clinical Genetics|April 5, 2019
Whole-exome sequencing revealed a nonsense mutation in STKLD1 causing non-syndromic pre-axial polydactyly type A affecting only upper limbMuhammad Umair, Muhammad Bilal, Raja H Ali, et al.Neurogenetics|July 25, 2015
In silico analysis of SIGMAR1 variant (rs4879809) segregating in a consanguineous Pakistani family showing amyotrophic lateral sclerosis without frontotemporal lobar dementiaMuhammad Ikram Ullah, Arsalan Ahmad, Syed Irfan Raza, et al.Life (Basel, Switzerland)|October 27, 2022
Polyphenols and Their Nanoformulations: Protective Effects against Human DiseasesSantosh Anand, Ramachandregowda Sowbhagya, Mohammad Azam Ansari, et al.European Journal of Human Genetics : EJHG|August 2, 2003
A locus for hereditary hypotrichosis localized to human chromosome 18q21.1Muhammad Arshad Rafique, Muhammad Ansar, Syed Muhammad Jamal, et al.Plants (Basel, Switzerland)|March 10, 2022
Quality Control Standardization, Contaminant Detection and In Vitro Antioxidant Activity of <i>Prunus domestica</i> Linn. FruitMohd Amir, Ameeduzzafar Zafar, Rizwan Ahmad, et al.Human Heredity|December 8, 2004
DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22Muhammad Ansar, Maria H Chahrour, Mohammad Amin Ud Din, et al.BMC Medical Genetics|December 13, 2007
Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequencesSajid Malik, K M Girisha, Muhammad Wajid, et al.Current Medicinal Chemistry|July 9, 2021
Epigenetics of Triple-Negative Breast Cancer via Natural CompoundsMohammed Kaleem, Maryam Perwaiz, Suza Mohammad Nur, et al.Pageof 34