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Affichage: 3 résultats.
    • Article de périodique
    Further delineation of the KAT6B molecular and phenotypic spectrum
    Gannon, Tamsin Perveen, Rahat Schlecht, Hélene Ramsden, Simon Anderson, Beverley Kerr, Bronwyn Day, Ruth Banka, Siddharth Suri, Mohnish Berland, Siren Gabbett, Michael Ma, Alan Lyonnet, Stan Cormier-Daire, Valerie Yilmaz, Rüstem Borck, Guntram Wieczorek, Dagmar Anderlid, Britt-Marie Smithson, Sarah Vogt, Julie Moore-Barton, Heather Simsek-Kiper, Pelin Ozlem Maystadt, Isabelle Destrée, Anne Bucher, Jessica Angle, Brad Mohammed, Shehla Wakeling, Emma Price, Sue Singer, Amihood Sznajer, Yves[UCL] Toutain, Annick Haye, Damien Newbury-Ecob, Ruth Fradin, Melanie McGaughran, Julie Tuysuz, Beyhan Tein, Mark Bouman, Katelijne Dabir, Tabib Van den Ende, Jenneke Luk, Ho Ming Pilz, Daniela T Eason, Jacqueline Davies, Sally Reardon, Willie Garavelli, Livia Zuffardi, Orsetta Devriendt, Koen Armstrong, Ruth Johnson, Diana Doco-Fenzy, Martine Bijlsma, Emilia Unger, Sheila Veenstra-Knol, Hermine E Kohlhase, Jürgen Lo, Ivan F M Smith, Janine Clayton-Smith, Jill (2015) European Journal of Human Genetics — Vol. 23, no. 9, p. 1165-1170 (2015)
    • Article de périodique
    How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum
    Banka, Siddharth Veeramachaneni, Ratna Reardon, William Howard, Emma Bunstone, Sancha Ragge, Nicola Parker, Michael J Crow, Yanick J Kerr, Bronwyn Kingston, Helen Metcalfe, Kay Chandler, Kate Magee, Alex Stewart, Fiona McConnell, Vivienne P M Donnelly, Deirdre E Berland, Siren Houge, Gunnar Morton, Jenny E Oley, Christine Revencu, Nicole[UCL] Park, Soo-Mi Davies, Sally J Fry, Andrew E Lynch, Sally Ann Gill, Harinder Schweiger, Susann Lam, Wayne W K Tolmie, John Mohammed, Shehla N Hobson, Emma Smith, Audrey Blyth, Moira Bennett, Christopher Vasudevan, Pradeep C García-Miñaúr, Sixto Henderson, Alex Goodship, Judith Wright, Michael J Fisher, Richard Gibbons, Richard Price, Susan M C de Silva, Deepthi Temple, I Karen Collins, Amanda L Lachlan, Katherine Elmslie, Frances McEntagart, Meriel Castle, Bruce Clayton-Smith, Jill Black, Graeme C Donnai, Dian (2012) European Journal of Human Genetics — Vol. 20, no.4, p. 381-388 (2011)
    • Article de périodique
    Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition.
    Palmer, Elizabeth E Pusch, Michael Picollo, Alessandra Forwood, Caitlin Nguyen, Matthew H Suckow, Vanessa Gibbons, Jessica Hoff, Alva Sigfrid, Lisa Megarbane, Andre Nizon, Mathilde Cogné, Benjamin Beneteau, Claire Alkuraya, Fowzan S Chedrawi, Aziza Hashem, Mais O Stamberger, Hannah Weckhuysen, Sarah Vanlander, Arnaud Ceulemans, Berten Rajagopalan, Sulekha Nunn, Kenneth Arpin, Stéphanie Raynaud, Martine Motter, Constance S Ward-Melver, Catherine Janssens, Katrien Meuwissen, Marije Beysen, Diane Dikow, Nicola Grimmel, Mona Haack, Tobias B Clement, Emma McTague, Amy Hunt, David Townshend, Sharron Ward, Michelle Richards, Linda J Simons, Cas Costain, Gregory Dupuis, Lucie Mendoza-Londono, Roberto Dudding-Byth, Tracy Boyle, Jackie Saunders, Carol Fleming, Emily El Chehadeh, Salima Spitz, Marie-Aude Piton, Amelie Gerard, Bénédicte Abi Warde, Marie-Thérèse Rea, Gillian McKenna, Caoimhe Douzgou, Sofia Banka, Siddharth Akman, Cigdem Bain, Jennifer M Sands, Tristan T Wilson, Golder N Silvertooth, Erin J Miller, Lauren Lederer, Damien Sachdev, Rani Macintosh, Rebecca Monestier, Olivier Karadurmus, Deniz Collins, Felicity Carter, Melissa Rohena, Luis Willemsen, Marjolein H Ockeloen, Charlotte W Pfundt, Rolph Kroft, Sanne D Field, Michael Laranjeira, Francisco E R Fortuna, Ana M Soares, Ana R Michaud, Vincent Naudion, Sophie Golla, Sailaja Weaver, David D Bird, Lynne M Friedman, Jennifer Clowes, Virginia Joss, Shelagh Pölsler, Laura Campeau, Philippe M Blazo, Maria Bijlsma, Emilia K Rosenfeld, Jill A Beetz, Christian Powis, Zöe McWalter, Kirsty Brandt, Tracy Torti, Erin Mathot, Mikaël[UCL] Mohammad, Shekeeb S Armstrong, Ruth Kalscheuer, Vera M (2023) Molecular psychiatry — Vol. 28, no. 2, p. 668-697 (2023)