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PRRT2-related phenotypes in patients with a 16p11.2 deletion.
Vlaskamp DRM, Callenbach PMC, Rump P, Giannini LAA, Brilstra EH, Dijkhuizen T, Vos YJ, van der Kevie-Kersemaekers AF, Knijnenburg J, de Leeuw N, van Minkelen R, Ruivenkamp CAL, Stegmann APA, Brouwer OF, van Ravenswaaij-Arts CMA. Vlaskamp DRM, et al. Among authors: brouwer of. Eur J Med Genet. 2019 Apr;62(4):265-269. doi: 10.1016/j.ejmg.2018.08.002. Epub 2018 Aug 17. Eur J Med Genet. 2019. PMID: 30125676 Free article.
Benign familial infantile convulsions: a clinical study of seven Dutch families.
Callenbach PM, de Coo RF, Vein AA, Arts WF, Oosterwijk J, Hageman G, ten Houten R, Terwindt GM, Lindhout D, Frants RR, Brouwer OF. Callenbach PM, et al. Among authors: brouwer of. Eur J Paediatr Neurol. 2002;6(5):269-83. doi: 10.1053/ejpn.2002.0609. Eur J Paediatr Neurol. 2002. PMID: 12374579 Free article.
Clinical and genetic aspects of idiopathic epilepsies in childhood.
Callenbach PM, van den Maagdenberg AM, Frants RR, Brouwer OF. Callenbach PM, et al. Among authors: brouwer of. Eur J Paediatr Neurol. 2005;9(2):91-103. doi: 10.1016/j.ejpn.2004.12.005. Eur J Paediatr Neurol. 2005. PMID: 15843076 Review.
209 results