المؤلفون: Abigail Atterbury, Nicola Improda, Angela Barnicoat, Nadia Schoenmakers, Senthil Senniappan, Caroline Ponmani, Krishna Chatterjee, Mehul T. Dattani

المصدر: Hormone research in paediatrics. 88(2)

مصطلحات موضوعية: 0301 basic medicine, Male, congenital, hereditary, and neonatal diseases and abnormalities, endocrine system, medicine.medical_specialty, endocrine system diseases, Adolescent, Endocrinology, Diabetes and Metabolism, medicine.medical_treatment, 030209 endocrinology & metabolism, urologic and male genital diseases, Thyroglobulin, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, Internal medicine, Non compliance, Congenital Hypothyroidism, Medicine, Adrenal adenoma, Humans, Congenital adrenal hyperplasia, Child, biology, Adrenal Hyperplasia, Congenital, business.industry, 21-Hydroxylase, medicine.disease, Phenotype, Congenital hypothyroidism, Pedigree, 030104 developmental biology, Pediatrics, Perinatology and Child Health, Mutation (genetic algorithm), Mutation, biology.protein, Patient Compliance, Female, business, hormones, hormone substitutes, and hormone antagonists

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::757dc562ebb4351fbbb1926a9805ead3Test
https://pubmed.ncbi.nlm.nih.gov/28359061Test

المؤلفون: Improda, Nicola, Ponmani, Caroline, Schoenmakers, Nadia, Senniappan, Senthil, Atterbury, Abigail, Barnicoat, Angela, Chatterjee, Krishna, Dattani, Mehul T.

المصدر: Hormone Research in Paediatrics; Sep2017, Vol. 88 Issue 2, p172-178, 7p, 1 Color Photograph, 1 Diagram, 1 Chart

مصطلحات موضوعية: ADRENOGENITAL syndrome, CONGENITAL hypothyroidism, GENETIC mutation, THERAPEUTICS