Koolen, David A ;
Pfundt, Rolph ;
Linda, Katrin...
Koolen , D A , Pfundt , R , Linda , K , Beunders , G , Veenstra-Knol , H E , Conta , J H , Fortuna , A M , Gillessen-Kaesbach , G , Dugan , S , Halbach , S , Abdul-Rahman , O A , Winesett , H M , Chung , W K , Dalton , M , Dimova , P S , Mattina , T , Prescott , K , Zhang , H Z , Saal , H M , Hehir-Kwa , J Y , Willemsen , M H , Ockeloen , C W , Jongmans , M C , Van der Aa , N , Failla , P , Barone , C , Avola , E , Brooks , A S , Kant , S G , Gerkes , E H , Firth , H V , Ounap , K , Bird , L M , Masser-Frye , D , Friedman , J R , Sokunbi , M A , Dixit , A , Splitt , M , Kukolich , M K , McGaughran , J , Coe , B P , Florez , J , Kasri , N N , Brunner , H G , Thompson , E M , Gecz , J , Romano , C , Eichler , E E & de Vries , B B A 2016 , ' The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant ' , European Journal of Human Genetics , vol. 24 , no. 5 , pp. 652-659 . https://doi.org/10.1038/ejhg.201....
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2016
