Sobering, Andrew K ;
Bryant, Laura M ;
Li, Dong...
Sobering , A K , Bryant , L M , Li , D , McGaughran , J , Maystadt , I , Moortgat , S , Graham , J M , van Haeringen , A , Ruivenkamp , C , Cuperus , R , Vogt , J , Morton , J , Brasch-Andersen , C , Steenhof , M , Hansen , L K , Adler , É , Lyonnet , S , Pingault , V , Sandrine , M , Ziegler , A , Donald , T , Nelson , B , Holt , B , Petryna , O , Firth , H , McWalter , K , Zyskind , J , Telegrafi , A , Juusola , J , Person , R , Bamshad , M J , Earl , D , Tsai , A C H , Yearwood , K R , Marco , E , Nowak , C , Douglas , J , Hakonarson , H , Bhoj , E J & University of Washington Center for Mendelian Genomics 2022 , ' Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology ' , Human Genetics and Genomics Advances , vol. 3 , no. 3 , 100102 . https://doi.org/10.1016/j.xhgg.2022.100102.
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2022
