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Ultrasound in Obstetrics & Gynecology, ISSN 0960-7692, 10/2019, Volume 54, Issue S1, pp. 400 - 401
Journal Article
Journal of Veterinary Internal Medicine, ISSN 0891-6640, 07/2015, Volume 29, Issue 4, pp. 1036 - 1044
Journal Article
Journal of Veterinary Internal Medicine, ISSN 0891-6640, 03/2016, Volume 30, Issue 2, pp. 591 - 601
Journal Article
Lancet, The, ISSN 0140-6736, 2010, Volume 375, Issue 9719, pp. 985 - 997
Journal Article
Journal of Dental Research, ISSN 0022-0345, 6/2019, Volume 98, Issue 6, pp. 659 - 665
This study investigated the genetic basis of an unusual autosomal dominant phenotype characterized by familial absent uvula, with a short posterior border of... 
craniofacial biology/genetics | cleft palate | transcription factor(s) | speech pathology | oral pathology | gene expression | craniofacial biology | genetics | Research Reports
Journal Article
by van der Sluijs, E.P.J and Jansen, S and Vergano, S.A and Adachi-Fukuda, M and Alanay, Yasemin and AlKindy, A and Baban, A and Bayat, A and Beck-Wödl, S and Berry, K and Bijlsma, Emilia and Bok, Levinus and Brouwer, A.F.J and Burgt, Ineke and Campeau, P.M and Canham, Natalie and Chrzanowska, Krystyna and Chu, Y.W.Y and Chung, B.H.Y and Dahan, Karin and De Rademaeker, M and Destrée, Anne and Dudding-Byth, T and Earl, R and Elcioglu, Nursel and Elias, E.R and Fagerberg, C and Gardham, Alice and Gener, B and Gerkes, Erica H and Grasshoff, Ute and Haeringen, Arie and Heitink, K.R and Herkert, Johanna and Hollander, Nicolette and Horn, Denise and Hunt, D and Kant, Sarina and Kato, M and Kayserili, Hülya and Kersseboom, Rogier and Kilic, E and Krajewska-Walasek, Malgorzata and Lammers, K and Laulund, L.W and Lederer, Damien and Lees, Melissa and López-González, V and Maas, Saskia and Mancini, Grazia and Marcelis, Carlo and Martinez, F and Maystadt, Isabelle and McGuire, M and McKee, S and Mehta, S and Metcalfe, Kay and Milunsky, Jeff and Mizuno, S and Moeschler, J.B and Netzer, C and Ockeloen, Charlotte and Oehl-Jaschkowitz, B and Okamoto, N and Olminkhof, S.N.M and Orellana, C and Pasquier, L and Pottinger, C and Riehmer, V and Robertson, Stephen and Roifman, M and Rooryck, Caroline and Ropers, F.G and Rosello, M and Ruivenkamp, Claudia and Sagiroglu, M.S and Sallevelt, Suzanne and Sanchis Calvo, A and Simsek-Kiper, P and Soares, Gabriela and Solaeche, L and Mujgan Sonmez, F and Splitt, M and Steenbeek, D and Stegmann, A.P.A and Stumpel, Connie and Tanabe, S and Uctepe, E and Utine, G.E and Veenstra-Knol, Hermine and Venkateswaran, S and Vilain, Catheline and Vincent-Delorme, Catherine and Vulto-van Silfhout, Anneke and Wheeler, P and Wilson, G.N and Wilson, Louise and Wollnik, B and Kosho, T and Wieczorek, Dagmar and ...
Genetics in Medicine, ISSN 1098-3600, 01/2018
textabstractPurpose: Pathogenic variants in ARID1B are one of the most frequent causes of intellectual disability (ID) as determined by large-scale exome... 
Coffin–Siris syndrome | ARID1B | intellectual disability | bias
Journal Article
Physics Reports, ISSN 0370-1573, 2006, Volume 427, Issue 5, pp. 257 - 454
Journal Article
Veterinary Pathology, ISSN 0300-9858, 5/2017, Volume 54, Issue 3, pp. 484 - 489
Journal Article
Journal of Veterinary Internal Medicine, ISSN 0891-6640, 03/2012, Volume 26, Issue 2, pp. 282 - 293
Journal Article