E. Mengen Et Al. , "A NOVEL FRAMESHIFT MUTATION IN ESCO2 GENE CAUSE ROBERTS SYNDROME: CASE PRESENTATION," HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.381, 2017
Mengen, E. Et Al. 2017. A NOVEL FRAMESHIFT MUTATION IN ESCO2 GENE CAUSE ROBERTS SYNDROME: CASE PRESENTATION. HORMONE RESEARCH IN PAEDIATRICS , vol.88 , 381.
Mengen, E., KOTAN, L. D., TOPALOĞLU, A. K., & YÜKSEL, B., (2017). A NOVEL FRAMESHIFT MUTATION IN ESCO2 GENE CAUSE ROBERTS SYNDROME: CASE PRESENTATION. HORMONE RESEARCH IN PAEDIATRICS , vol.88, 381.
Mengen, Eda Et Al. "A NOVEL FRAMESHIFT MUTATION IN ESCO2 GENE CAUSE ROBERTS SYNDROME: CASE PRESENTATION," HORMONE RESEARCH IN PAEDIATRICS , vol.88, 381, 2017
Mengen, Eda Et Al. "A NOVEL FRAMESHIFT MUTATION IN ESCO2 GENE CAUSE ROBERTS SYNDROME: CASE PRESENTATION." HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.381, 2017
Mengen, E. Et Al. (2017) . "A NOVEL FRAMESHIFT MUTATION IN ESCO2 GENE CAUSE ROBERTS SYNDROME: CASE PRESENTATION." HORMONE RESEARCH IN PAEDIATRICS , vol.88, p.381.
@article{article, author={Eda Mengen Et Al. }, title={A NOVEL FRAMESHIFT MUTATION IN ESCO2 GENE CAUSE ROBERTS SYNDROME: CASE PRESENTATION}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2017, pages={381} }