Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment

Author:

Carlson A.D,Obeid J.S,Kanellopoulou N,Wilson R.C,New M.I

Publisher

Elsevier BV

Subject

Cell Biology,Clinical Biochemistry,Endocrinology,Molecular Biology,Molecular Medicine,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference23 articles.

1. Genetic disorders of steroid metabolism;New,1995

2. Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Pang;Pediatrics,1988

3. Newborn screening, prenatal diagnosis, and prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Pang;Trends Endocrinol. Metab.,1990

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

5. High frequency of non-classical steroid 21-hydroxylase deficiency;Speiser;Am. J. Hum. Genet.,1985

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