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机译:Hirschsprung病患者中的复合遗传:缺乏基因功能障碍不足的渗透
Capital Inst Pediat Beijing Municipal Key Lab Child Dev &
Nutri Dept Med Genet Beijing 100020;
Shanghai Jiao Tong Univ Shanghai Inst Pediat Res Shanghai Key Lab Pediat Gastroenterol &
Nutr;
Univ Chinese Acad Sci Shanghai Inst Nutr &
Hlth Chinese Acad Sci Shanghai Inst Biol Sci CAS MPG;
Capital Inst Pediat Beijing Municipal Key Lab Child Dev &
Nutri Dept Med Genet Beijing 100020;
Affiliated Childrens Hosp Dept Gen Surg Capital Inst Pediat 2 Yabao Rd Beijing 100020 Peoples;
Affiliated Childrens Hosp Dept Gen Surg Capital Inst Pediat 2 Yabao Rd Beijing 100020 Peoples;
Univ Chinese Acad Sci Shanghai Inst Nutr &
Hlth Chinese Acad Sci Shanghai Inst Biol Sci CAS MPG;
Shanghai Jiao Tong Univ Shanghai Inst Pediat Res Shanghai Key Lab Pediat Gastroenterol &
Nutr;
Affiliated Childrens Hosp Dept Gen Surg Capital Inst Pediat 2 Yabao Rd Beijing 100020 Peoples;
机译:中国孤立性巨sch病患者RET,EDNRB和EDN3基因及MCS + 9.7中三个SNP的遗传分析
机译:中国散发性巨结肠疾病患者的高度复发性RET突变和受体酪氨酸激酶和内皮素B通路基因的新突变
机译:中国大肠埃希氏病患者RET基因的突变
机译:缺血性心脏病患者内皮功能障碍药物治疗的新见解。
机译:解开微胶质基因Trem2的功能障碍如何增加阿尔茨海默病的风险
机译:中国大肠埃希氏病患者RET基因的突变
机译:中国先天性巨结肠患者RET基因突变
机译:心力衰竭:左心室收缩功能障碍患者的评估和护理。临床实践指南第11号;心力衰竭:左心室收缩功能障碍患者的治疗。临床医生快速参考指南第11号;与心脏病共存:是心衰吗?患者和家庭指南