The Arid1b Spectrum In 143 Patients: From Nonsyndromic Intellectual Disability To Coffin-Siris Syndrome (Vol 21, Pg 1295, 2019)
Pleuntje J. Van Der Sluijs,Sandra Jansen,Samantha A. Vergano,Miho Adachi-Fukuda,Yasemin Alanay,Adila Alkindy,Anwar Baban,Allan Bayat,Stefanie Beck-Woedl,Katherine Berry,Emilia K. Bijlsma,Levinus A. Bok, Alwin F. J. Brouwer,Ineke Van Der Burgt,Philippe M. Campeau,Natalie Canham,Krystyna Chrzanowska, Yoyo W. Y. Chu,Brain H. Y. Chung,Karin Dahan,Marjan De Rademaeker,Anne Destree,Tracy Dudding-Byth,Rachel Earl,Nursel Elcioglu,Ellen R. Elias,Christina Fagerberg,Alice Gardham,Blanca Gener,Erica H. Gerkes,Ute Grasshoff,Arie Van Haeringen,Karin R. Heitink,Johanna C. Herkert,Nicolette S. Den Hollander,Denise Horn,David Hunt,Sarina G. Kant,Mitsuhiro Kato,Hulya Kayserili,Rogier Kersseboom,Esra Kilic,Malgorzata Krajewska-Walasek,Kylin Lammers,Lone W. Laulund,Damien Lederer,Melissa Lees,Vanesa Lopez-Gonzalez,Saskia Maas,Grazia M. S. Mancini,Carlo Marcelis,Francisco Martinez,Isabelle Maystadt,Marianne Mcguire,Shane Mckee,Sarju Mehta,Kay Metcalfe,Jeff Milunsky,Seiji Mizuno,John B. Moeschler,Christian Netzer,Charlotte W. Ockeloen,Barbara Oehl-Jaschkowitz,Nobuhiko Okamoto, Sharon N. M. Olminkhof,Carmen Orellana,Laurent Pasquier,Caroline Pottinger,Vera Riehmer,Stephen P. Robertson,Maian Roifman,Caroline Rooryck,Fabienne G. Ropers,Monica Rosello,Claudia A. L. Ruivenkamp,Mahmut S. Sagiroglu,Suzanne C. E. H. Sallevelt,Amparo Sanchis Calvo,Pelin O. Simsek-Kiper,Gabriela Soares,Lucia Solaeche,Fatma Mujgan Sonmez,Miranda Splitt,Duco Steenbeek,Alexander P. A. Stegmann,Constance T. R. M. Stumpel,Saori Tanabe,Eyyup Uctepe,G. Eda Utine,Hermine E. Veenstra-Knol,Sunita Venkateswaran,Catheline Vilain,Catherine Vincent-Delorme,Anneke T. Vulto-Van Silfhout,Patricia Wheeler,Golder N. Wilson,Louise C. Wilson,Bernd Wollnik,Tomoki Kosho,Dagmar Wieczorek,Evan Eichler,Rolph Pfundt,Bert B. A. De Vries,Jill Clayton-Smith,Gijs W. E. Santen
GENETICS IN MEDICINE（2019）
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