Results 351 to 360 of about 2,389,640 (367)
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The Genetics of 21-Hydroxylase Deficiency
The Endocrinologist, 1994Phyllis W. Speiser, Javier Aisenberg
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Female Pseudohermaphroditism in 21-Hydroxylase Deficiency
1987Congenital adrenal hyperplasia (CAH) is a family of inherited disorders of adrenal steroidogenesis. Each of these disorders has a characteristic pattern of hormonal abnormalities caused by an inherited deficiency of one of the several enzymes necessary for normal steroid synthesis.
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Molecular analysis of the 21‐hydroxylase gene
Clinical Endocrinology, 2003Alicia Belgorosky +2 more
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Prenatal diagnosis of 21‐hydroxylase deficiency
Prenatal Diagnosis, 1988Cynthia Callaway +2 more
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Steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia
Journal of Steroid Biochemistry and Molecular Biology, 2017A. Parsa, M. New
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Cardio-metabolic risk factors in youth with classical 21-hydroxylase deficiency
European Journal of Pediatrics, 2017Kansuda Ariyawatkul +3 more
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THE MOLECULAR GENETICS OF 21-HYDROXYLASE DEFICIENCY
Annual Review of Genetics, 1989Walter L. Miller, Yves Morel
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Autoimmune Addison's disease and 21-hydroxylase
The Lancet, 1992J. Bednarek +7 more
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A new ELISA for autoantibodies to steroid 21-hydroxylase
Clinical Chemistry and Laboratory Medicine, 2017Maria del Pilar Larosa +11 more
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