A. Topaloglu Et Al. , "Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G," JOURNAL OF INHERITED METABOLIC DISEASE , vol.22, no.1, pp.82-83, 1999
Topaloglu, A. Et Al. 1999. Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G. JOURNAL OF INHERITED METABOLIC DISEASE , vol.22, no.1 , 82-83.
Topaloglu, A., Sansaricq, C., Fox, J., Bale, A., Tuchman, M., & Desnick, R., (1999). Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G. JOURNAL OF INHERITED METABOLIC DISEASE , vol.22, no.1, 82-83.
Topaloglu, ALİ Et Al. "Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G," JOURNAL OF INHERITED METABOLIC DISEASE , vol.22, no.1, 82-83, 1999
Topaloglu, ALİ K. Et Al. "Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G." JOURNAL OF INHERITED METABOLIC DISEASE , vol.22, no.1, pp.82-83, 1999
Topaloglu, A. Et Al. (1999) . "Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G." JOURNAL OF INHERITED METABOLIC DISEASE , vol.22, no.1, pp.82-83.
@article{article, author={ALİ KEMAL TOPALOĞLU Et Al. }, title={Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G}, journal={JOURNAL OF INHERITED METABOLIC DISEASE}, year=1999, pages={82-83} }