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Publications by S Collier

Molecular Pathology of 21-Hydroxylase Deficiency

Pediatric Research

English

Related publications

Dna Hybridization Analysis of 21-Hydroxylase Deficiency

Pediatric Research

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Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients With 21-Hydroxylase Deficiency

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Location of the Gene for 21-Hydroxylase Deficiency

Pediatric Research

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HLA Class I-, Complement C4- And 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency

Clinical Chemistry and Laboratory Medicine

Clinical Biochemistry

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Genetics and Biochemical Variability of Variants of 21 Hydroxylase Deficiency.

Journal of Medical Genetics

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Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

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111 Cah (21-Hydroxylase Deficiency) Presenting as Central Precocious Puberty

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Late Onset 21-Hydroxylase Deficiency Presenting as Pre-Pubertal Gynaecomastia

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21-Hydroxylase Deficiency Families With HLA Identical Affected and Unaffected Sibs.

Journal of Medical Genetics

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