N. M. Sahin Et Al. , "Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.30, no.8, pp.889-892, 2017
Sahin, N. M. Et Al. 2017. Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.30, no.8 , 889-892.
Sahin, N. M., Bilici, M. E., Kurnaz, E., Akdogan, M. P., Ceylaner, S., & AYCAN, Z., (2017). Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.30, no.8, 889-892.
Sahin, Nursel Et Al. "Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.30, no.8, 889-892, 2017
Sahin, Nursel M. Et Al. "Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.30, no.8, pp.889-892, 2017
Sahin, N. M. Et Al. (2017) . "Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.30, no.8, pp.889-892.
@article{article, author={Nursel Muratoglu Sahin Et Al. }, title={Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2017, pages={889-892} }