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Publications by C. Nelson-Williams
Hypertension With or Without Adrenal Hyperplasia Due to Different Inherited Mutations in the Potassium Channel KCNJ5
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Finding Genetic Contributions to Sporadic Disease: A Recessive Locus at 12q24 Commonly Contributes to Patent Ductus Arteriosus
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Related publications
Cushing Syndrome Due to Macronodular Adrenal Hyperplasia
Congenital Adrenal Hyperplasia Due to Cytochrome P450 Oxidoreductase Deficiency
Correction: Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency: Functional Consequences of Four CYP11B1 Mutations
European Journal of Human Genetics
Genetics
Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency
Mutations in the CYP11B1 Gene Causing Congenital Adrenal Hyperplasia and Hypertension Cluster in Exons 6, 7, and 8.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Prevalence of Testicular Adrenal Rest Tumours in Male Children With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
L-Type Calcium Channel Mutations in Japanese Patients With Inherited Arrhythmias
Circulation Journal
Medicine
Cardiovascular Medicine
Cardiology
Hypertension Due to Gain-Of-Function Mutations in the Mineralocorticoid Receptor
