Browsing by Author Maas, S

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TitleAuthor(s)Issue DateViews
 
Exome sequencing of a pedigree with Caudal Regression Syndrome (CRS)
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
Cheng, GWong, EHMSham, PCCherny, SSMaas, SScherer, SWMarshall, CRPereira, SLTam, PKHGarcia-Barcelo, MM
2012
84
 
The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome
Journal:Genetics In Medicine
van der Sluijs, EJansen, SVergano, SAAdachi-Fukuda, MAlanay, TAlkindy, ABaban, ABayat, ABeck-Woddl, SBerry, KBijsma, EKNetzer, COckeloen, CWOehl-Jaschkowitz, BOkamoto, NOlminkhof, SNMOrellana, CPasquier, LPottinger, CRiehmer, VRobertson, SPRoifman, MRooryck, CRopers, FGRosello, MRuivenkamp, CALSagiroglu, MSSallevelt, SCEHSanchis Calvo, ASimsek-Kipser, POSoares, GSolaeche, LMujgan Sonmez, FSplitt, MSteenbeek, DStegmann, APAStumpel, CTRMTanabe, SUctepe, EUtine, GEVeenstra-Knol, HEVenkateswaran, SVilain, CVincent-Delorme, CVulto-van Silfhout, ATWheeler, PWilson, GNWilson, LCWollnik, BKosho, TWieczorek, DEichler, EPfundt, Rde Vries, BBAClayuton-Smith, JSanten, GWEBok, LABrouwer, AFJvab der Burgt, ICampeau, PMCanham, NChrzanowska, KChu, WYChung, BHYDahan, KDe Rademaeker, MDestree, ADudding-Byth, TEarl, RElcioglu, NElias, ERFagerberg, CGardham, AGener, BGerkes, EHGrasshoff, Uvan Haeringen, AHeitink, KRHerkert, JCden Hollander, NSHorn, DHunt, DKant, SGKato, MKayserili, HKersseboom, RKilic, EKrajewska-Walasek, MLammers, KLaulund, LWLederer, DLees, MLopez-Gonzalez, VMaas, SMancini, GMSMarcelis, CMartinez, FMaystadt, IMcGuire, MMcKee, SMehta, SMetcalfe, KMilunsky, JMizuno, SMoeschler, JB
2018
111
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