A rapid screening for steroid 21-hydroxylase mutations in patients with congenital adrenal hyperplasia [PDF]
Klaus Kapelari +6 more
openalex +1 more source
Spontaneous Pregnancy in Genetically Confirmed 11-Beta Hydroxylase Deficiency: A Case Series and Literature Review. [PDF]
Machineni P +4 more
europepmc +1 more source
Measurement of twenty-one serum steroid profiles by UPLC-MS/MS for the diagnosis and monitoring of congenital adrenal hyperplasia. [PDF]
Lee JH +6 more
europepmc +1 more source
Mutation of IVS2 –12A/C>G in Combination with 707–714delGAGACTAC in the CYP21 Gene Is Caused by Deletion of the C4-CYP21 Repeat Module with Steroid 21-Hydroxylase Deficiency [PDF]
Hsien-Hsiung Lee +4 more
openalex +1 more source
Endocrine consequences of antifungal therapy: A missed entity. [PDF]
Thakkar S +6 more
europepmc +1 more source
Associations between polymorphism of the steroid 21-hydroxylase gene (<i>CYP21</i>) and litter size of Polish Large White × Polish Landrace sows* (short communication) [PDF]
Joanna Ziemak, Wilhelm Grzesiak
openalex +1 more source
Analysis of Autoantibody Epitopes on Steroid 21-Hydroxylase Using a Panel of Monoclonal Antibodies1 [PDF]
Shu Chen +11 more
openalex +1 more source
Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency. [PDF]
Yousaf S +5 more
europepmc +1 more source

