Evaluation of 7 patients form 3 families with isolated growth hormone deficiency due to two different GHRHR function loss mutations

---

KURNAZ E., SAVAŞ ERDEVE Ş., Legendre m., bayramoglu e., muratoglu sahin n., keskin m., ...More

10th International Meeting of Pediatric Endocrinology, 14 - 17 September 2017, (Summary Text)

• Publication Type: Conference Paper / Summary Text
• Ankara University Affiliated: No