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المؤلفون: Yuan Chen, Guli Amuti, Kaidi Zhang, Xiangxin Song, Munila Abudounaiyimu, Jing Wang, Jun Jiang, Xinling Wang, Jimilanmu Maimaitiming, Yanying Guo, Adila Alimu, AiHeMaiTiJiang TuHuTi
المصدر: Pharmacogenomics and Personalized Medicine
مصطلحات موضوعية: 0301 basic medicine, Proband, congenital, hereditary, and neonatal diseases and abnormalities, Pediatrics, medicine.medical_specialty, Offspring, media_common.quotation_subject, Gene mutation, Sister, 03 medical and health sciences, 0302 clinical medicine, Pharmacogenomics and Personalized Medicine, non-classical 21-hydroxylase deficiency, medicine, congenital adrenal hyperplasia, Congenital adrenal hyperplasia, gene mutation, Original Research, media_common, Pharmacology, Daughter, biology, business.industry, 21-Hydroxylase, CYP21A2 gene, medicine.disease, Brother, 030104 developmental biology, 030220 oncology & carcinogenesis, biology.protein, Molecular Medicine, business
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