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Congenital Anomalies|April 21, 2017
Novel sequence variants in the LIPH and LPAR6 genes underlies autosomal recessive woolly hair/hypotrichosis in consanguineous familiesFarooq Ahmad, Salma Sharif, Muhammad Furqan Ubaid, et al.
Clinical Genetics|October 23, 2022
A novel variant in AFF3 underlying isolated syndactylyHammal Khan, Glenn Koh, Angie En Qi Chong, et al.
Journal of Cataract and Refractive Surgery|October 15, 2021
Nondiffractive wavefront-shaping extended depth-of-focus intraocular lens: visual performance and patient-reported outcomesThomas Kohnen, Kerstin Petermann, Myriam Böhm, et al.
American Journal of Medical Genetics. Part A|March 22, 2005
Autosomal recessive mesoaxial synostotic syndactyly with phalangeal reduction maps to chromosome 17p13.3Sajid Malik, Ferda E Percin, Wasim Ahmad, et al.
Artificial Cells, Nanomedicine, and Biotechnology|April 11, 2020
A comparative pulmonary pharmacokinetic study of budesonide using polymeric nanoparticles targeted to the lungs in treatment of asthmaNiyaz Ahmad, Rizwan Ahmad, Mortaja Zaki Almakhamel, et al.
Indian Journal of Pediatrics|May 20, 2018
Prevalence of Depression among Caregivers of Indian Children with Cystic FibrosisJaveed Iqbal Bhat, Wasim Ahmad Wani, Bashir A Charoo, et al.
European Journal of Human Genetics : EJHG|May 11, 2017
Exome sequencing revealed a splice site variant in the IQCE gene underlying post-axial polydactyly type A restricted to lower limbMuhammad Umair, Khadim Shah, Bader Alhaddad, et al.
Scientific Reports|March 15, 2024
Identification of kidney stones in KUB X-ray images using VGG16 empowered with explainable artificial intelligenceFahad Ahmed, Sagheer Abbas, Atifa Athar, et al.
Journal of Human Genetics|February 21, 2009
Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3Muhammad Salman Chishti, Kwanghyuk Lee, Merry-Lynn McDonald, et al.
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