Search Results - "Adachi-Fukuda Miho"

  • Showing 1 - 2 results of 2
Refine Results
  1. 1

    The ARID1B phenotype: What we have learned so far by Santen, Gijs W.E., Clayton-Smith, Jill

    “…Evidence is now accumulating from a number of sequencing studies that ARID1B not only appears to be one of the most frequently mutated intellectual disability…”
    Get full text
    Journal Article
  2. 2

    Correction: The ARID1B spectrum in 143 patients: fromnonsyndromic intellectual disability to Coffin–Siris syndrome by Jansen, Sandra, Vergano Samantha A, Adachi-Fukuda Miho, Alanay Yasemin, AlKindy Adila, Baban Anwar, Bayat, Allan, Beck-Wödl Stefanie, Berry, Katherine, Bijlsma, Emilia K, Bok, Levinus A, Brouwer Alwin F J, van der Burgt Ineke, Campeau, Philippe M, Canham, Natalie, Chrzanowska Krystyna, Chu Yoyo W Y, Chung Brain H Y, Dahan, Karin, De, Rademaeker Marjan, Destree Anne, Dudding-Byth Tracy, Earl, Rachel, Elcioglu Nursel, Elias, Ellen R, Gardham Alice, Gener Blanca, Gerkes, Erica H, Grasshoff Ute, van Haeringen Arie, Heitink, Karin R, Herkert, Johanna C, den Hollander Nicolette S, Horn, Denise, Hunt, David, Kato Mitsuhiro, Kayserili Hülya, Kersseboom Rogier, Kilic Esra, Krajewska-Walasek Malgorzata, Lammers Kylin, Laulund, Lone W, Lederer, Damien, Lees, Melissa, López-González Vanesa, Maas Saskia, Mancini, Grazia M, Marcelis, Carlo, Martinez, Francisco, Maystadt Isabelle, McGuire, Marianne, McKee, Shane, Mehta Sarju, Metcalfe, Kay, Milunsky, Jeff, Mizuno Seiji, Moeschler, John B, Netzer, Christian, Ockeloen, Charlotte W, Oehl-Jaschkowitz Barbara, Okamoto Nobuhiko, Olminkhof Sharon N M, Pasquier, Laurent, Pottinger, Caroline, Riehmer Vera, Robertson, Stephen P, Roifman Maian, Rooryck Caroline, Ropers, Fabienne G, Rosello, Monica, Ruivenkamp Claudia A L, Sagiroglu, Mahmut S, Sallevelt Suzanne C E H, Calvo, Amparo Sanchis, Simsek-Kiper, Pelin O, Soares, Gabriela, Solaeche Lucia, Sonmez Fatma Mujgan, Splitt Miranda, Steenbeek Duco, Stegmann Alexander P A, Stumpel Constance T R M, Tanabe Saori, Eyyup, Uctepe, Eda, Utine G, Veenstra-Knol, Hermine E, Venkateswaran Sunita, Vilain Catheline, Vincent-Delorme, Catherine, Wheeler, Patricia, Wilson, Golder N, Wilson, Louise C, Wollnik Bernd, Kosho Tomoki, Wieczorek Dagmar, Eichler, Evan, Rolph, Pfundt, de Vries Bert B A, Clayton-Smith, Jill, Santen Gijs W E

    Published in Genetics in medicine (01-09-2019)
    “…The original version of this Article contained an error in the spelling of the author Pleuntje J. van der Sluijs, which was incorrectly given as Eline (P. J.)…”
    Get full text
    Journal Article