KARACA, E. Et Al. 2015. Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.167, no.11 , 2795-2799.

KARACA, E., YUREGIR, O. O., Bozdogan, S. T., Aslan, H., PEHLIVAN, D., JHANGIANI, S. N., ... AKDEMIR, Z. C.(2015). Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.167, no.11, 2795-2799.

KARACA, SEVCAN Et Al. "Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome," AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.167, no.11, 2795-2799, 2015

KARACA, SEVCAN T. Et Al. "Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.167, no.11, pp.2795-2799, 2015

KARACA, E. Et Al. (2015) . "Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.167, no.11, pp.2795-2799.

@article{article, author={SEVCAN TUĞ BOZDOĞAN Et Al. }, title={Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome}, journal={AMERICAN JOURNAL OF MEDICAL GENETICS PART A}, year=2015, pages={2795-2799} }