MIHÇI, E. Et Al. 2012. Wolcott-Rallison Syndrome Due to a Novel Mutation (R491X) in EIF2AK3 Gene. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.4, no.2 , 101-103.

MIHÇI, E., TURKKAHRAMAN, D., Ellard, S., Akcurin, S., & Bircan, I., (2012). Wolcott-Rallison Syndrome Due to a Novel Mutation (R491X) in EIF2AK3 Gene. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.4, no.2, 101-103.

MIHÇI, ERCAN Et Al. "Wolcott-Rallison Syndrome Due to a Novel Mutation (R491X) in EIF2AK3 Gene," JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.4, no.2, 101-103, 2012

MIHÇI, ERCAN Et Al. "Wolcott-Rallison Syndrome Due to a Novel Mutation (R491X) in EIF2AK3 Gene." JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.4, no.2, pp.101-103, 2012

MIHÇI, E. Et Al. (2012) . "Wolcott-Rallison Syndrome Due to a Novel Mutation (R491X) in EIF2AK3 Gene." JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.4, no.2, pp.101-103.

@article{article, author={ERCAN MIHÇI Et Al. }, title={Wolcott-Rallison Syndrome Due to a Novel Mutation (R491X) in EIF2AK3 Gene}, journal={JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY}, year=2012, pages={101-103} }