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Publications by Nazli B. McDonnell
Complement Component 4 Copy Number Variation and CYP21A2 Genotype Associations in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Human Genetics
Genetics
The Phenotypic Spectrum of Contiguous Deletion ofCYP21A2and Tenascin XB: Quadricuspid Aortic Valve and Other Midline Defects
American Journal of Medical Genetics, Part A
Genetics
Related publications
Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Genotype-Phenotype Correlation in 1,507 Families With Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency
Psychological Vulnerability to Stress in Carriers of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Hormones
Medicine
Endocrinology
Metabolism
Diabetes
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
Long-Term Glucocorticoid Effect on Bone Mineral Density in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Steroid 21-Hydroxylase Deficiency in Mice. An Animal Model for Congenital Adrenal Hyperplasia.
Proceedings of The Japanese Association of Animal Models for Human Diseases
Novel Variants of CYP21A2 in Vietnamese Patients With Congenital Adrenal Hyperplasia
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Deletion of the 21-Hydroxylase Gene in Congenital Adrenal Hyperplasia
Pediatric Research
Child Health
Pediatrics
Perinatology
