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Molecular Vision|August 2, 2017
Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous familiesAsmat Ullah, Muhammad Umair, Maryam Yousaf, et al.European Journal of Human Genetics : EJHG|December 24, 2015
Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disabilityMuhammad Ansar, Abid Jan, Regie Lyn P Santos-Cortez, et al.International Journal of Dermatology|November 14, 2017
Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous familiesKhadim Shah, Sabba Mehmood, Abid Jan, et al.Frontiers in Medicine|September 16, 2024
The genetic cause of neurodevelopmental disorders in 30 consanguineous familiesSohail Aziz Paracha, Shoaib Nawaz, Muhammad Tahir Sarwar, et al.European Journal of Human Genetics : EJHG|December 11, 2014
Challenges and solutions for gene identification in the presence of familial locus heterogeneityAtteeq U Rehman, Regie Lyn P Santos-Cortez, Meghan C Drummond, et al.Pageof 3