Six 11-Beta Hydroxylase Deficiency Patients: Identification of Two Novel Mutations

Onay, H�seyin; I��k, Esra; �zen, Samim; Kavaso�lu, Ay�e Nur; Y�ld�r�m �im�ir, Ilg�n; Atik, Tahir; Sarer Y�rekli, Banu; Yavuz, Hazal; Ba�ol, �brahim; Darcan, ��kran; �zk�nay, Ferda

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Turkish Society for Pediatric Endocrinology and Diabetes

Six 11-Beta Hydroxylase Deficiency Patients: Identification of Two Novel Mutations [J Clin Res Pediatr Endocrinol]

J Clin Res Pediatr Endocrinol. 2017; 9(1): 26-26

Six 11-Beta Hydroxylase Deficiency Patients: Identification of Two Novel Mutations

H�seyin Onay¹, Esra I��k², Samim �zen³, Ay�e Nur Kavaso�lu¹, Ilg�n Y�ld�r�m �im�ir⁴, Tahir Atik², Banu Sarer Y�rekli⁴, Hazal Yavuz¹, �brahim Ba�ol¹, ��kran Darcan³, Ferda �zk�nay²
¹Ege University Faculty Of Medicine, Department Of Medical Genetics, Izmir, Turkey
²Ege University Faculty Of Medicine, Division Of Pediatric Genetics, Izmir, Turkey
³Ege University Faculty Of Medicine, Division Of Pediatric Endocrinology, Izmir, Turkey
⁴Ege University Faculty Of Medicine, Department Of Endocrinology, Izmir, Turkey

H�seyin Onay, Esra I��k, Samim �zen, Ay�e Nur Kavaso�lu, Ilg�n Y�ld�r�m �im�ir, Tahir Atik, Banu Sarer Y�rekli, Hazal Yavuz, �brahim Ba�ol, ��kran Darcan, Ferda �zk�nay. Six 11-Beta Hydroxylase Deficiency Patients: Identification of Two Novel Mutations. J Clin Res Pediatr Endocrinol. 2017; 9(1): 26-26
Manuscript Language: English

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