Search Results - Umair, Muhammad

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    Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations by Werren, Elizabeth A. (Author) , Peirent, Emily R. (Author) , Jantti, Henna (Author) , Guxholli, Alba (Author) , Srivastava, Kinshuk Raj (Author) , Orenstein, Naama (Author) , Narayanan, Vinodh (Author) , Wiszniewski, Wojciech (Author) , Dawidziuk, Mateusz (Author) , Gawlinski, Pawel (Author) , Umair, Muhammad (Author) , Khan, Amjad (Author) , Khan, Shahid Niaz (Author) , Geneviève, David (Author) , Lehalle, Daphné (Author) , van Gassen, K. L. I. (Author) , Giltay, Jacques C. (Author) , Oegema, Renske (Author) , van Jaarsveld, Richard H. (Author) , Rafiullah, Rafiullah (Author) , Rappold, Gudrun (Author) , Rabin, Rachel (Author) , Pappas, John G. (Author) , Wheeler, Marsha M. (Author) , Bamshad, Michael J. (Author) , Tsan, Yao-Chang (Author) , Johnson, Matthew B. (Author) , Keegan, Catherine E. (Author) , Srivastava, Anshika (Author) , Bielas, Stephanie L. (Author) ,


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    Two cases of recessive intellectual disability caused by NDST1 and METTL23 variants by Khan, Amjad (Author) , Miao, Zhichao (Author) , Umair, Muhammad (Author) , Ullah, Amir (Author) , Alshabeeb, Mohammad A. (Author) , Bilal, Muhammad (Author) , Ahmad, Farooq (Author) , Rappold, Gudrun (Author) , Ansar, Muhammad (Author) , Carapito, Raphael (Author) ,


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