Krall, M., Htun, S., Schnur, R. E., Brooks, A. S., Baker, L., de Alba Campomanes, A., . . . Slavotinek, A. M. (2019). Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomalies. Eur J Hum Genet.
Styl cytowania ChicagoKrall, Max, et al. "Biallelic Sequence Variants in INTS1 in Patients With Developmental Delays, Cataracts, and Craniofacial Anomalies." Eur J Hum Genet 2019.
Styl cytowania MLAKrall, Max, et al. "Biallelic Sequence Variants in INTS1 in Patients With Developmental Delays, Cataracts, and Craniofacial Anomalies." Eur J Hum Genet 2019.
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