Novel Rapid Molecular Diagnosis Methods for Comprehensive Genetic Analysis of 21-Hydroxylase Deficiency
Orphanet Journal of Rare Diseases（2024）
关键词
Congenital adrenal hyperplasia,21-OHD,SNaPshot,CNVplex,Genetic analysis
AI 理解论文
溯源树
样例
生成溯源树，研究论文发展脉络
Chat Paper
正在生成论文摘要