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Human Genetics|October 27, 2006
Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3Shahid Y Khan, Saima Riazuddin, Muhammad Tariq, et al.
Human Genome Variation|May 16, 2020
Mutations in CERKL and RP1 cause retinitis pigmentosa in Pakistani familiesRaheela Nadeem, Firoz Kabir, Jiali Li, et al.
American Journal of Human Genetics|August 28, 2010
A mutation in ZNF513, a putative regulator of photoreceptor development, causes autosomal-recessive retinitis pigmentosaLin Li, Naoki Nakaya, Venkata R M Chavali, et al.
Saudi Journal of Biological Sciences|September 30, 2020
Peripheral blood T cells response in human parainfluenza virus-associated lower respiratory tract infection in childrenAisha Gul, Sanaullah Khan, Muhammad Arshad, et al.
Saudi Journal of Biological Sciences|November 11, 2021
Evaluation of analgesic, antiamnesic and antidiarrheal potentials of Medicago denticulata extract using animal modelSaeed Ahmad, Sanaullah Khan, Alam Zeb, et al.
BMC Medical Genetics|February 11, 2011
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndromeSaima Riazuddin, Zubair M Ahmed, Rashmi S Hegde, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|March 24, 2012
Hepatitis E virus-associated aplastic anaemia: the first case of its kindShahida Amjad Riaz Shah, Amreek Lal, Muhammad Idrees, et al.
Critical Reviews in Eukaryotic Gene Expression|September 30, 2021
Dengue Vaccines: Ongoing Challenges and Current Status in the Advancement of Different CandidatesMuhammad Hassan, Ali Hassan, Muhammad Farooq, et al.
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