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Publications by D. Chitayat
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
Prolonged Duration of Persistent Cell Free Fetal DNA From a Vanishing Twin
Ultrasound in Obstetrics and Gynecology
Nuclear Medicine
Radiology
Ultrasound Technology
Gynecology
Reproductive Medicine
Radiological
Imaging
Obstetrics
Medicine
Related publications
Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
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
Psychological Vulnerability to Stress in Carriers of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Hormones
Medicine
Endocrinology
Metabolism
Diabetes
Complement Component 4 Copy Number Variation and CYP21A2 Genotype Associations in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Human Genetics
Genetics
Steroid 21-Hydroxylase Deficiency in Mice. An Animal Model for Congenital Adrenal Hyperplasia.
Proceedings of The Japanese Association of Animal Models for Human Diseases
Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency
Deletion of the 21-Hydroxylase Gene in Congenital Adrenal Hyperplasia
Pediatric Research
Child Health
Pediatrics
Perinatology
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
Molecular Analysis of a Family With Congenital Adrenal Hyperplasia - Genotype/Phenotype Discrepancy
Balkan Journal of Medical Genetics
Genetics
