Yilmaz, S. Et Al. 2018. Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome. MOLECULAR GENETICS & GENOMIC MEDICINE , vol.6, no.2 , 230-248.

Yilmaz, S., ULUDAĞ ALKAYA, D., KASAPÇOPUR, Ö., BARUT, K., Akdemir, E. S., Celen, C., ... Youngblood, M. W.(2018). Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome. MOLECULAR GENETICS & GENOMIC MEDICINE , vol.6, no.2, 230-248.

Yilmaz, Saliha Et Al. "Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome," MOLECULAR GENETICS & GENOMIC MEDICINE , vol.6, no.2, 230-248, 2018

Yilmaz, Saliha Et Al. "Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome." MOLECULAR GENETICS & GENOMIC MEDICINE , vol.6, no.2, pp.230-248, 2018

Yilmaz, S. Et Al. (2018) . "Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome." MOLECULAR GENETICS & GENOMIC MEDICINE , vol.6, no.2, pp.230-248.

@article{article, author={Saliha Yilmaz Et Al. }, title={Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome}, journal={MOLECULAR GENETICS & GENOMIC MEDICINE}, year=2018, pages={230-248} }