Demirhan, O. Et Al. 2005. A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies. JOURNAL OF MEDICAL GENETICS , vol.42, no.4 , 314-317.

Demirhan, O., TURKMEN, S., SCHWABE, G., SOYUPAK, S., AKGUL, E., TASTEMIR, D., ... KARAHAN, D.(2005). A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies. JOURNAL OF MEDICAL GENETICS , vol.42, no.4, 314-317.

Demirhan, OSMAN Et Al. "A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies," JOURNAL OF MEDICAL GENETICS , vol.42, no.4, 314-317, 2005

Demirhan, OSMAN Et Al. "A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies." JOURNAL OF MEDICAL GENETICS , vol.42, no.4, pp.314-317, 2005

Demirhan, O. Et Al. (2005) . "A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies." JOURNAL OF MEDICAL GENETICS , vol.42, no.4, pp.314-317.

@article{article, author={OSMAN DEMİRHAN Et Al. }, title={A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies}, journal={JOURNAL OF MEDICAL GENETICS}, year=2005, pages={314-317} }