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Publications by Ana Elisa C. Billerbeck

Use of Nonradioactive Labeling to Detect Large Gene Rearrangements in 21-Hydroxylase Deficiency

Revista do Hospital das Clínicas
2004English

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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

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Molecular Pathology of 21-Hydroxylase Deficiency

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Dna Hybridization Analysis of 21-Hydroxylase Deficiency

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Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

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

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Psychological Vulnerability to Stress in Carriers of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

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Genetics and Biochemical Variability of Variants of 21 Hydroxylase Deficiency.

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

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