Kolvenbach, Caroline M ;
Dworschak, Gabriel C ;
Frese, Sandra...
Kolvenbach , C M , Dworschak , G C , Frese , S , Japp , A S , Schuster , P , Wenzlitschke , N , Yilmaz , O , Lopes , F , Pryalukhin , A , Schierbaum , L , van der Zanden , L F M , Kause , F , Schneider , R , Taranta-Janusz , K , Szczepanska , M , Pawlaczyk , K , Newman , W G , Beaman , G M , Stuart , H M , Cervellione , R , Feitz , W F J , van Rooij , I A L M , Schreuder , M F , Steffens , M , Weber , S , Merz , W M , Feldkotter , M , Hoppe , B , Thiele , H , Altmuller , J , Berg , C , Kristiansen , G , Ludwig , M , Reutter , H , Woolf , A S , Hilderbrandt , F , Grote , P , Zaniew , M , Odermatt , B & Hilger , A C 2019 , ' Rare Variants in BNC2 are implicated in autosomal dominant congenital lower urinary tract obstruction ' , American Journal of Human Genetics . https://doi.org/10.1016/j.ajhg.2019.03.023.
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2019
