Acta Obstetricia et Gynecologica Scandinavica, 100(11), 2036-2043. Wiley Acta Obstetricia et Gynecologica Scandinavica, 100(11), 2036-2043. Wiley-Blackwell Acta Obstetricia et Gynecologica Scandinavica, 100(11), 2036-2043. WILEY Srebniak, M I, Jehee, F S, Joosten, M, Boter, M, de Valk, W G, van der Helm, R, Sistermans, E A, Voorhoeve, E, Bhola, S, Hoffer, M J V, den Hollander, N, Macville, M V E & van Opstal, D 2021, ' Non-invasive prenatal diagnosis for translocation carriers—YES please or NO go? ', Acta Obstetricia et Gynecologica Scandinavica, vol. 100, no. 11, pp. 2036-2043 . https://doi.org/10.1111/aogs.14256, https://doi.org/10.1111/aogs.14256 Acta Obstetricia et Gynecologica Scandinavica
Genetics in Medicine, 21(6), 1295-1307. Nature Publishing Group GENETICS IN MEDICINE r-FISABIO. Repositorio Institucional de Producción Científica instname Genetics in Medicine Genetics in Medicine, 21, 6, pp. 1295-1307 Genetics in Medicine, 21(6), 1295-1307. Lippincott Williams & Wilkins Genetics in medicine, 21(6), 1295-1307. Lippincott Williams and Wilkins Genetics in Medicine, 21, 1295-1307 Genetics in Medicine, 21(6), 1295-1307. NATURE PUBLISHING GROUP r-FISABIO: Repositorio Institucional de Producción Científica Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO) Clayton-Smith, J & et al 2018, ' The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome ', Genetics in Medicine . https://doi.org/10.1038/s41436-018-0330-z van der Sluijs, E P J, Jansen, S, Vergano, S A, Adachi-Fukuda, M, Alanay, Y, AlKindy, A, Baban, A, Bayat, A, Beck-Wödl, S, Berry, K, Bijlsma, E K, Bok, L A, Brouwer, A F J, van der Burgt, I, Campeau, P M, Canham, N, Chrzanowska, K, Chu, Y W Y, Chung, B H Y, Dahan, K, De Rademaeker, M, Destree, A, Dudding-Byth, T, Earl, R, Elcioglu, N, Elias, E R, Fagerberg, C, Gardham, A, Gener, B, Gerkes, E H, Grasshoff, U, van Haeringen, A, Heitink, K R, Herkert, J C, den Hollander, N S, Horn, D, Hunt, D, Kant, S G, Kato, M, Kayserili, H, Kersseboom, R, Kilic, E, Krajewska-Walasek, M, Lammers, K, Laulund, L W, Lederer, D, Lees, M, López-González, V, Maas, S, Mancini, G M S, Marcelis, C, Martinez, F, Maystadt, I, McGuire, M, McKee, S, Mehta, S, Metcalfe, K, Milunsky, J, Mizuno, S, Moeschler, J B, Netzer, C, Ockeloen, C W, Oehl-Jaschkowitz, B, Okamoto, N, Olminkhof, S N M, Orellana, C, Pasquier, L, Pottinger, C, Riehmer, V, Robertson, S P, Roifman, M, Rooryck, C, Ropers, F G, Rosello, M, Ruivenkamp, C A L, Sagiroglu, M S, Sallevelt, S C E H, Sanchis Calvo, A, Simsek-Kiper, P O, Soares, G, Solaeche, L, Sonmez, F M, Splitt, M, Steenbeek, D, Stegmann, A P A, Stumpel, C T R M, Tanabe, S, Uctepe, E, Utine, G E, Veenstra-Knol, H E, Venkateswaran, S, Vilain, C, Vincent-Delorme, C, Vulto-van Silfhout, A T, Wheeler, P, Wilson, G N, Wilson, L C, Wollnik, B, Kosho, T, Wieczorek, D, Eichler, E, Pfundt, R, de Vries, B B A, Clayton-Smith, J & Santen, G W E 2019, ' The ARID1B spectrum in 143 patients : from nonsyndromic intellectual disability to Coffin-Siris syndrome ', Genetics in Medicine, vol. 21, no. 6, pp. 1295-1307 . https://doi.org/10.1038/s41436-018-0330-z r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
Genetics in Medicine, 21(5), 1074-1082. Lippincott Williams & Wilkins Genetics in Medicine, 21(5), 1074-1082 Genetics in Medicine Genetics in medicine, 21(5), 1074-1082. Lippincott Williams and Wilkins
AMERICAN JOURNAL OF HUMAN GENETICS r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe instname American Journal of Human Genetics American Journal of Human Genetics, Elsevier (Cell Press), 2021, 108 (5), pp.929-941. ⟨10.1016/j.ajhg.2021.03.017⟩ American Journal of Human Genetics, 108(5), 929-941. CELL PRESS American Journal of Human Genetics, 2021, 108 (5), pp.929-941. ⟨10.1016/j.ajhg.2021.03.017⟩ Am J Hum Genet