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Clinical Dysmorphology|August 31, 2019
A novel missense variant in the BBS7 gene underlying Bardet-Biedl syndrome in a consanguineous Pakistani familyAmir Hayat, Atif Ahmad Khan, Abdur Rauf, et al.
The Australasian Journal of Dermatology|March 18, 2014
Mutations in the lipase-H gene causing autosomal recessive hypotrichosis and woolly hairSabba Mehmood, Abid Jan, Dost Muhammad, et al.
Indian Journal of Pediatrics|May 24, 2017
Flexible Bronchoscopy in Non-resolving PneumoniaJaveed Iqbal Bhat, Wasim Ahmad Wani, Qazi Iqbal Ahmad, et al.
Medicina (Kaunas, Lithuania)|December 23, 2022
Exome Sequencing Revealed a Novel Splice Site Variant in the <i>CRB2</i> Gene Underlying Nephrotic SyndromeAnam Simaab, Jai Krishin, Sultan Rashid Alaradi, et al.
Saudi Journal of Biological Sciences|March 14, 2022
Lipid peroxidation reduction and hippocampal and cortical neurons protection against ischemic damage in animal model using <i>Stellaria media</i>Wasim Ahmad, Mushtaq Ahmad, Muhammad Umar Khayam Sahibzada, et al.
The Journal of Gene Medicine|August 28, 2023
A variant in sperm-specific glycolytic enzyme enolase 4 (ENO4) causes human male infertilityShoaib Nawaz, Shabir Hussain, Muhammad Bilal, et al.
Pediatrics and Neonatology|August 11, 2018
Vitamin D status correlates with the markers of cystic fibrosis-related pulmonary diseaseWasim Ahmad Wani, Mudasir Nazir, Javeed Iqbal Bhat, et al.
European Journal of Medical Genetics|August 15, 2018
A novel insertion and deletion mutation in the BHLHA9 underlies polydactyly and mesoaxial synostotic syndactyly with phalangeal reductionAsmat Ullah, Raja Hussain Ali, Ayesha Isani Majeed, et al.
Chemistry & Biodiversity|April 8, 2025
Nutritional, Medicinal, and Commercial Significance of Moringa oleifera L. Leaves: A Comprehensive ReviewHarshita Barkat, Bushra Riaz, Afreen Fatima, et al.
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