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Publications by P A Dyer
21-Hydroxylase Deficiency Families With HLA Identical Affected and Unaffected Sibs.
Journal of Medical Genetics
Genetics
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HLA and Hormonal Studies in Families of Patients With 21-Hydroxylase Deficiency - Cryptic Patients?
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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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Remarkably Similar Response to Gold Therapy in HLA Identical Sibs With Rheumatoid Arthritis.
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Genotype-Phenotype Correlation in 1,507 Families With Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency
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Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients With 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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Location of the Gene for 21-Hydroxylase Deficiency
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Clinical Course of Patients With Nonclassical 21-Hydroxylase Deficiency (21-Ohd) Diagnosed in Infancy and Childhood
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