R. Yilmaz Et Al. , "Kaufman oculocerebrofacial syndrome: Novel UBE3B mutations and clinical features in four unrelated patients," AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.176, no.1, pp.187-193, 2018
Yilmaz, R. Et Al. 2018. Kaufman oculocerebrofacial syndrome: Novel UBE3B mutations and clinical features in four unrelated patients. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.176, no.1 , 187-193.
Yilmaz, R., SZAKSZON, K., ALTMANN, A., Altunoglu, U., Senturk, L., MCGUIRE, M., ... CALABRESE, O.(2018). Kaufman oculocerebrofacial syndrome: Novel UBE3B mutations and clinical features in four unrelated patients. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.176, no.1, 187-193.
Yilmaz, Ruestem Et Al. "Kaufman oculocerebrofacial syndrome: Novel UBE3B mutations and clinical features in four unrelated patients," AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.176, no.1, 187-193, 2018
Yilmaz, Ruestem Et Al. "Kaufman oculocerebrofacial syndrome: Novel UBE3B mutations and clinical features in four unrelated patients." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.176, no.1, pp.187-193, 2018
Yilmaz, R. Et Al. (2018) . "Kaufman oculocerebrofacial syndrome: Novel UBE3B mutations and clinical features in four unrelated patients." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.176, no.1, pp.187-193.
@article{article, author={Ruestem Yilmaz Et Al. }, title={Kaufman oculocerebrofacial syndrome: Novel UBE3B mutations and clinical features in four unrelated patients}, journal={AMERICAN JOURNAL OF MEDICAL GENETICS PART A}, year=2018, pages={187-193} }