Frints, Suzanna G. M ;
Hennig, Friederike ;
Colombo, Roberto...
Frints , S G M , Hennig , F , Colombo , R , Jacquemont , S , Terhal , P , Zimmerman , H H , Hunt , D , Mendelsohn , B A , Kordaß , U , Webster , R , Sinnema , M , Abdul-Rahman , O , Suckow , V , Fernández-Jaén , A , van Roozendaal , K , Stevens , S J C , Macville , M V E , Al-Nasiry , S , van Gassen , K , Utzig , N , Koudijs , S M , McGregor , L , Maas , S M , Baralle , D , Dixit , A , Wieacker , P , Lee , M , Lee , A S , Engle , E C , Houge , G , Gradek , G A , Douglas , A G L , Longman , C , Joss , S , Velasco , D , Hennekam , R C , Hirata , H & Kalscheuer , V M 2019 , ' Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita ' , Human Mutation , vol. 40 , no. 12 , pp. 2270-2285 . https://doi.org/10.1002/humu.23841.
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2019
