Search Results - Narayanan, Vinodh

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    De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies by Weisz-Hubshman, Monika (Author) , Burrage, Lindsay C. (Author) , Jangam, Sharayu V. (Author) , Rosenfeld, Jill A. (Author) , Hardenberg, Sandra von (Author) , Bergmann, Anke (Author) , Richter, Manuela Friederike (Author) , Rydzanicz, Malgorzata (Author) , Ploski, Rafal (Author) , Stembalska, Agnieszka (Author) , Chung, Wendy K. (Author) , Hernan, Rebecca R. (Author) , Lim, Foong Y. (Author) , Brunet, Theresa (Author) , Syrbe, Steffen (Author) , Keren, Boris (Author) , Heide, Solveig (Author) , Murdock, David R. (Author) , Dai, Hongzheng (Author) , Xia, Fan (Author) , Ketkar, Shamika (Author) , Dawson, Brian (Author) , Narayanan, Vinodh (Author) , Graves, Hillary K. (Author) , Wangler, Michael F. (Author) , Bacino, Carlos (Author) , Lee, Brendan (Author) ,


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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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