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 - United States
doi 10.1073/pnas.1300057110
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Proceedings of the National Academy of Sciences

Related search

Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

2020English

Prevalence of Testicular Adrenal Rest Tumours in Male Children With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

European Journal of Endocrinology
MedicineEndocrinologyMetabolismDiabetes
2007English

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

Hormones
MedicineEndocrinologyMetabolismDiabetes
2017English

Complement Component 4 Copy Number Variation and CYP21A2 Genotype Associations in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Human Genetics
Genetics
2012English

Steroid 21-Hydroxylase Deficiency in Mice. An Animal Model for Congenital Adrenal Hyperplasia.

Proceedings of The Japanese Association of Animal Models for Human Diseases
1991English

Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency

2020English

Deletion of the 21-Hydroxylase Gene in Congenital Adrenal Hyperplasia

Pediatric Research
Child HealthPediatricsPerinatology
1986English

Long-Term Glucocorticoid Effect on Bone Mineral Density in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

European Journal of Endocrinology
MedicineEndocrinologyMetabolismDiabetes
2016English

Molecular Analysis of a Family With Congenital Adrenal Hyperplasia - Genotype/Phenotype Discrepancy

Balkan Journal of Medical Genetics
Genetics
2007English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy