Mengen, E. Et Al. 2017. COMBINATION OF HIRSCHSPRUNG DISEASE AND A NOVEL DEFINED MUTATION RELATED CONGENITAL ADRENAL HYPERPLASIA IN CYP21A2 GENE: CASE PRESENTATION. HORMONE RESEARCH IN PAEDIATRICS , vol.88 , 432.

Mengen, E., KOTAN, L. D., TOPALOĞLU, A. K., & YÜKSEL, B., (2017). COMBINATION OF HIRSCHSPRUNG DISEASE AND A NOVEL DEFINED MUTATION RELATED CONGENITAL ADRENAL HYPERPLASIA IN CYP21A2 GENE: CASE PRESENTATION. HORMONE RESEARCH IN PAEDIATRICS , vol.88, 432.

Mengen, Eda Et Al. "COMBINATION OF HIRSCHSPRUNG DISEASE AND A NOVEL DEFINED MUTATION RELATED CONGENITAL ADRENAL HYPERPLASIA IN CYP21A2 GENE: CASE PRESENTATION," HORMONE RESEARCH IN PAEDIATRICS , vol.88, 432, 2017

Mengen, Eda Et Al. "COMBINATION OF HIRSCHSPRUNG DISEASE AND A NOVEL DEFINED MUTATION RELATED CONGENITAL ADRENAL HYPERPLASIA IN CYP21A2 GENE: CASE PRESENTATION." HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.432, 2017

Mengen, E. Et Al. (2017) . "COMBINATION OF HIRSCHSPRUNG DISEASE AND A NOVEL DEFINED MUTATION RELATED CONGENITAL ADRENAL HYPERPLASIA IN CYP21A2 GENE: CASE PRESENTATION." HORMONE RESEARCH IN PAEDIATRICS , vol.88, p.432.

@article{article, author={Eda Mengen Et Al. }, title={COMBINATION OF HIRSCHSPRUNG DISEASE AND A NOVEL DEFINED MUTATION RELATED CONGENITAL ADRENAL HYPERPLASIA IN CYP21A2 GENE: CASE PRESENTATION}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2017, pages={432} }