机译:22 Q11.2在22Q11.2中对先天性心脏病的低可血症缺失综合征
Divisions of Endocrinology and DiabetesThe Children's Hospital of Philadelphia and the Perelman;
Divisions of Endocrinology and DiabetesThe Children's Hospital of Philadelphia and the Perelman;
Human GeneticsThe Children's Hospital of Philadelphia and the Perelman School of Medicine at the;
Divisions of Endocrinology and DiabetesThe Children's Hospital of Philadelphia and the Perelman;
Human GeneticsThe Children's Hospital of Philadelphia and the Perelman School of Medicine at the;
Division of CardiologyThe Children's Hospital of Philadelphia and the Perelman School of Medicine;
Human GeneticsThe Children's Hospital of Philadelphia and the Perelman School of Medicine at the;
Human GeneticsThe Children's Hospital of Philadelphia and the Perelman School of Medicine at the;
congenital heart disease; hypocalcemia22q11.2 microdeletion;
机译:22 Q11.2在22Q11.2中对先天性心脏病的低可血症缺失综合征
机译:22Q11.2删除综合征在先天性心脏病与脊柱侧凸之间的关系中的作用
机译:22Q11.2删除综合征和先天性心脏病
机译:制定患者综合征先天性心脏病的治疗决策:需要循证医学
机译:基于家庭的遗传关联研究中的统计问题,并应用于唐氏综合症的先天性心脏缺陷。
机译:低钙血症与先天性心脏病在22q11.2缺失综合征中的关联
机译:22 Q11.2在22Q11.2中具有先天性心脏病的低可血症的关联综合征