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作 者:王莉 WANG Li(Genetic&Prenatal Diag Center,1st Affil Hosp,Zhengzhou Univ,Zhengzhou 450052)
机构地区:[1]Genetic&Prenatal Diag Center,1st Affil Hosp,Zhengzhou Univ,Zhengzhou 450052
出 处:《China Medical Abstracts(Internal Medicine)》2024年第1期53-54,共2页中国医学文摘(内科学分册(英文版)
摘 要:Objective To detect and analyze the gene variation types of 64 unrelated pedigrees affected with autosomal dominant polycystic kidney disease (ADPKD),and explore the detection efficiency of multiple gene analysis techniques and variation characteristics.Methods The clinical data of 64 pedigrees with ADPKD from Nephrology Department or Genetic and Prenatal Diagnosis Center of the First Affiliated Hospital of Zhengzhou University from December 2017 to August 2020 were retrospectively analyzed.
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