Eggermann, T., Begemann, M., & Pfeiffer, L. (2021). Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with an impact on both imprinting domains. Clin Epigenetics.
Chicago Style citaatEggermann, Thomas, Matthias Begemann, en Lutz Pfeiffer. "Unusual Deletion of the Maternal 11p15 Allele in Beckwith–Wiedemann Syndrome With an Impact On Both Imprinting Domains." Clin Epigenetics 2021.
MLA citatieEggermann, Thomas, Matthias Begemann, en Lutz Pfeiffer. "Unusual Deletion of the Maternal 11p15 Allele in Beckwith–Wiedemann Syndrome With an Impact On Both Imprinting Domains." Clin Epigenetics 2021.
Let op: Deze citaties zijn niet altijd 100% accuraat.