American Journal of Human Genetics, 108(7), 1342-1349. Cell Press Repositório Científico de Acesso Aberto de Portugal Repositório Científico de Acesso Aberto de Portugal (RCAAP) instacron:RCAAP American Journal of Human Genetics, 108, 7, pp. 1342-1349 American Journal of Human Genetics, 108, 1342-1349 Am J Hum Genet
Genetics in Medicine, 23(7), 1246-1254. Lippincott Williams & Wilkins Genetics in Medicine, 23, 1246-1254 Genetics in Medicine, 23, 7, pp. 1246-1254 Genet Med
Genetics in Medicine, 23, 4, pp. 645-652 Polla, DL, Bhoj, EJ, Verheij, JBGM, Wassink-Ruiter, JSK, Reis, A, Deshpande, C, Gregor, A, Hill-Karfe, K, Silfhout, ATV, Pfundt, R, Bongers, EMHF, Hakonarson, H & de, B APM 2020, ' De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females ', Genetics in medicine : official journal of the American College of Medical Genetics . https://doi.org/10.1038/s41436-020-01040-6 Genetics in Medicine, 23(4), 645-652. Nature Publishing Group Genetics in Medicine, 23, 645-652
Am J Hum Genet American journal of human genetics, Vol. 107, no.1, p. 164-172 (2020) American Journal of Human Genetics, 107(1), 164-172. Cell Press American Journal of Human Genetics, 107(1), 164-172. CELL PRESS The American Journal of Human Genetics American Journal of Human Genetics, 107, 164-172 American Journal of Human Genetics, 107, 1, pp. 164-172