Bogliş, A., Cosma, A. S., Tripon, F., & Bãnescu, C. (2020). Exon 21 deletion in the OPHN1 gene in a family with syndromic X-linked intellectual disability: Case report. Medicine (Baltimore).
Chicago ZitierstilBogliş, Alina, Adriana S. Cosma, Florin Tripon, und Claudia Bãnescu. "Exon 21 Deletion in the OPHN1 Gene in a Family With Syndromic X-linked Intellectual Disability: Case Report." Medicine (Baltimore) 2020.
MLA ZitierstilBogliş, Alina, Adriana S. Cosma, Florin Tripon, und Claudia Bãnescu. "Exon 21 Deletion in the OPHN1 Gene in a Family With Syndromic X-linked Intellectual Disability: Case Report." Medicine (Baltimore) 2020.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.