Erdem, M. Et Al. 2019. Long-Term Follow-Up of a Case with Dyskeratosis Congenita Caused by NHP2-V126M/X154R Mutation: Genotype-Phenotype Association. ACTA HAEMATOLOGICA , vol.141, no.1 , 28-31.

Erdem, M., TÜFEKÇİ, Ö., YILMAZ, Ş., ALACACIOĞLU, İ., & ÖREN, H., (2019). Long-Term Follow-Up of a Case with Dyskeratosis Congenita Caused by NHP2-V126M/X154R Mutation: Genotype-Phenotype Association. ACTA HAEMATOLOGICA , vol.141, no.1, 28-31.

Erdem, Melek Et Al. "Long-Term Follow-Up of a Case with Dyskeratosis Congenita Caused by NHP2-V126M/X154R Mutation: Genotype-Phenotype Association," ACTA HAEMATOLOGICA , vol.141, no.1, 28-31, 2019

Erdem, Melek Et Al. "Long-Term Follow-Up of a Case with Dyskeratosis Congenita Caused by NHP2-V126M/X154R Mutation: Genotype-Phenotype Association." ACTA HAEMATOLOGICA , vol.141, no.1, pp.28-31, 2019

Erdem, M. Et Al. (2019) . "Long-Term Follow-Up of a Case with Dyskeratosis Congenita Caused by NHP2-V126M/X154R Mutation: Genotype-Phenotype Association." ACTA HAEMATOLOGICA , vol.141, no.1, pp.28-31.

@article{article, author={Melek Erdem Et Al. }, title={Long-Term Follow-Up of a Case with Dyskeratosis Congenita Caused by NHP2-V126M/X154R Mutation: Genotype-Phenotype Association}, journal={ACTA HAEMATOLOGICA}, year=2019, pages={28-31} }