机译:骨质疏松症 - 假性综合征患者LRP5 LRP5基因中的新突变
Folkh?lsan Institute of GeneticsUniversity of HelsinkiHelsinki Finland;
Center for Molecular MedicineKarolinska University HospitalStockholm Sweden;
Erciyes UniversityDepartment of Pediatric EndocrinologyTurkey;
Department of Clinical GeneticsChristian Medical College and Hospital VelloreIndia;
IntergenGenetic Diagnosis Research and Application CenterAnkara Turkey;
Erciyes UniversityDepartment of Pediatric EndocrinologyTurkey;
Department of Clinical GeneticsChristian Medical College and Hospital VelloreIndia;
Dr.Sami Ulus Children's HospitalDepartment of Pediatric EndocrinologyAnkara Turkey;
Dr.Sami Ulus Children's HospitalDepartment of Pediatric EndocrinologyAnkara Turkey;
Department of Clinical GeneticsChristian Medical College and Hospital VelloreIndia;
Department of Woman and Child HealthAstrid Lindgren Children's Hospital at Karolinska University;
Folkh?lsan Institute of GeneticsUniversity of HelsinkiHelsinki Finland;
机译:骨质疏松症 - 假性综合征患者LRP5 LRP5基因中的新突变
机译:影响骨质疏松-假性神经胶质瘤综合征(OPPG)患者LRP5剪接的新型突变。
机译:四例骨质疏松症-假性神经胶质瘤综合征患者的各种LRP5突变:使用寡核苷酸切片微阵列鉴定7.2-kb的微缺失。
机译:新加坡巴鲁达综合征患者SCN5A基因突变的谱
机译:内皮细胞中的Norrin,Frizzled-4和Lrp5信号控制着视网膜血管化的遗传程序。
机译:新型突变影响骨质疏松-假性神经胶质瘤综合征(OPPG)患者的LRP5剪接
机译:新型突变影响骨质疏松-假性神经胶质瘤综合征(OPPG)患者的LRP5剪接