Genetics in medicine Genetics in Medicine, 24(10), 2112-2122. Lippincott Williams and Wilkins Genetics in Medicine, 24, 2112-2122 Genetics in Medicine, 24(10), 2112-2122. Nature Publishing Group Genetics in Medicine, 24(10), 2112-2122. ELSEVIER SCIENCE INC Genetics in Medicine, 24(10), 2112-2122. Lippincott Williams & Wilkins Genetics in Medicine, 24, 10, pp. 2112-2122 van den Bersselaar, L M, Verhagen, J M A, Bekkers, J A, Kempers, M, Houweling, A C, Baars, M, Overwater, E, Hilhorst-Hofstee, Y, Barge-Schaapveld, D Q C M, Rompen, E, Krapels, I P C, Dulfer, E, Wessels, M W, Loeys, B L, Verhagen, H J M, Maugeri, A, Roos-Hesselink, J W, Brüggenwirth, H T & van de Laar, I M B H 2022, ' Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort ', Genetics in Medicine, vol. 24, no. 10, pp. 2112-2122 . https://doi.org/10.1016/j.gim.2022.07.009 Genetics in medicine, 24(10), 2112-2122. Lippincott Williams and Wilkins
American journal of medical genetics. Part A, 191(2), 479-489. Wiley-Liss Inc. American Journal of Medical Genetics. Part A, 191, 2, pp. 479-489 The American Journal of Medical Genetics-Part A, 191(2), 479-489. WILEY American Journal of Medical Genetics, Part A, 191(2), 479-489. Wiley-Liss Inc. American Journal of Medical Genetics Part A, 191(2), 479-489. Wiley American Journal of Medical Genetics. Part A, 191, 479-489 American journal of medical genetics : part A American Journal of Medical Genetics, Part A, 191(2). Wiley American journal of medical genetics. Part A. Wiley-Liss Inc. Lauffer, P, Pals, G, Zwinderman, A H, Postema, F A M, Baars, M J H, Dulfer, E, Hilhorst-Hofstee, Y, Houweling, A C, Kempers, M, Krapels, I P C, van de Laar, I M B H, Loeys, B, Spaans, A M J, Warnink-Kavelaars, J, de Waard, V, Wit, J M & Menke, L A 2023, ' Growth charts for Marfan syndrome in the Netherlands and analysis of genotype–phenotype relationships ', American Journal of Medical Genetics, Part A, vol. 191, no. 2, pp. 479-489 . https://doi.org/10.1002/ajmg.a.63047
Journal of Medical Genetics, 59, 9, pp. 865-877 Journal of Medical Genetics, 59, 865-877 Journal of Medical Genetics, 59(9), 865-877. BMJ Publishing Group Journal of Medical Genetics. BMJ PUBLISHING GROUP Journal of Medical Genetics Minatogawa, M, Unzaki, A, Morisaki, H, Syx, D, Sonoda, T, Janecke, A R, Slavotinek, A, Voermans, N C, Lacassie, Y, Mendoza-Londono, R, Wierenga, K J, Jayakar, P, Gahl, W A, Tifft, C J, Figuera, L E, Hilhorst-Hofstee, Y, Maugeri, A, Ishikawa, K, Kobayashi, T, Aoki, Y, Ohura, T, Kawame, H, Kono, M, Mochida, K, Tokorodani, C, Kikkawa, K, Morisaki, T, Kobayashi, T, Nakane, T, Kubo, A, Ranells, J D, Migita, O, Sobey, G, Kaur, A, Ishikawa, M, Yamaguchi, T, Matsumoto, N, Malfait, F, Miyake, N & Kosho, T 2022, ' Clinical and molecular features of 66 patients with musculocontractural Ehlers-Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14) ', Journal of Medical Genetics, vol. 59, no. 9, pp. 865-877 . https://doi.org/10.1136/jmedgenet-2020-107623
Genetics in Medicine Genetics in Medicine, Nature Publishing Group, 2020, 22 (3), pp.524-537. ⟨10.1038/s41436-019-0657-0⟩ Genetics in medicine : official journal of the American College of Medical Genetics, vol 22, iss 3 Genetics in Medicine, 22(3), 524-537. Nature Publishing Group Genet Med Genetics in Medicine, 22(3), 524-537. NATURE PUBLISHING GROUP