Muratoǧlu Sahin, N. Et Al. 2017. Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation. Journal of Pediatric Endocrinology and Metabolism , vol.30, no.8 , 889-892.

Muratoǧlu Sahin, N., Bilici, M. E., Kurnaz, E., Pala Akdoǧan, M., CEYLANER, S., & AYCAN, Z., (2017). Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation. Journal of Pediatric Endocrinology and Metabolism , vol.30, no.8, 889-892.

Muratoǧlu Sahin, Nursel Et Al. "Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation," Journal of Pediatric Endocrinology and Metabolism , vol.30, no.8, 889-892, 2017

Muratoǧlu Sahin, Nursel M. Et Al. "Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation." Journal of Pediatric Endocrinology and Metabolism , vol.30, no.8, pp.889-892, 2017

Muratoǧlu Sahin, N. Et Al. (2017) . "Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation." Journal of Pediatric Endocrinology and Metabolism , vol.30, no.8, pp.889-892.

@article{article, author={Nursel Muratoǧlu Sahin Et Al. }, title={Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation}, journal={Journal of Pediatric Endocrinology and Metabolism}, year=2017, pages={889-892} }