SCIE

Bölükbaşı, E. Y., Afzal, M., Mümtaz, S., Ahmad, N., Malik, S., Tolun, A., "Progressive SCAR14 with Unclear Speech, Developmental Delay, Tremor, and Behavioral Problems Caused by a Homozygous Deletion of the SPTBN2 Pleckstrin Homology Domain", American Journal of Medical Genetics Part A, 173, 9, 2494-2499, 2017.

Türkçe

Berber, E., Özbil, M., Brown, C., Başlar, Z., Çaglayan, S. H., Lillicrap, D., "Functional Characterisation of the Type 1 von Willebrand Disease Candidate VWF Gene Variants: p. M771I, p. L881R and p. P1413L", Blood Transfusion, 15, 6, 548-556, 2017.

Türkçe

Sayfalar