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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