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Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3.
Acar S, BinEssa HA, Demir K, Al-Rijjal RA, Zou M, Çatli G, Anık A, Al-Enezi AF, Özışık S, Al-Faham MSA, Abacı A, Dündar B, Kattan WE, Alsagob M, Kavukçu S, Tamimi HE, Meyer BF, Böber E, Shi Y. Acar S, et al. Among authors: anik a. PLoS One. 2018 Mar 5;13(3):e0193388. doi: 10.1371/journal.pone.0193388. eCollection 2018. PLoS One. 2018. PMID: 29505567 Free PMC article.
46,XX male disorder of sexual development:a case report.
Anık A, Çatlı G, Abacı A, Böber E. Anık A, et al. J Clin Res Pediatr Endocrinol. 2013;5(4):258-60. doi: 10.4274/Jcrpe.1098. J Clin Res Pediatr Endocrinol. 2013. PMID: 24379036 Free PMC article.
133 results