Steroid 21 Hydroxylase Deficiency Congenital Adrenal Hyperplasia

Author:

Nimkarn Saroj,Lin-Su Karen,New Maria I.

Publisher

Elsevier BV

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference114 articles.

1. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: newborn screening and its relationship to the diagnosis and treatment of the disorder;Pang;Screening,1993

2. Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia;Therrell;Pediatrics,1998

3. Congenital adrenal hyperplasia: neonatal mass screening compared with clinical diagnosis only in the Emilia-Romagna region of Italy, 1980–1995;Balsamo;Pediatrics,1996

4. High frequency of nonclassical steroid 21-hydroxylase deficiency;Speiser;Am J Hum Genet,1985

5. A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency;Sherman;Am J Hum Genet,1988

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