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机译:家族性先天性脑积水的遗传景观
King Faisal Specialist Hosp &
Res Ctr Dept Genet Riyadh Saudi Arabia;
King Faisal Specialist Hosp &
Res Ctr Dept Genet Riyadh Saudi Arabia;
King Faisal Specialist Hosp &
Res Ctr Dept Genet Riyadh Saudi Arabia;
King Faisal Specialist Hosp &
Res Ctr Dept Genet Riyadh Saudi Arabia;
King Faisal Specialist Hosp &
Res Ctr Dept Obstet &
Gynecol Riyadh Saudi Arabia;
King Saud Univ Coll Med Dept Surg Riyadh Saudi Arabia;
King Fahad Gen Hosp Dept Med Genet Jeddah Saudi Arabia;
King Faisal Specialist Hosp &
Res Ctr Dept Obstet &
Gynecol Riyadh Saudi Arabia;
Secur Forces Hosp Dept Pediat Riyadh Saudi Arabia;
King Saud Univ Coll Med Dept Pediat Riyadh 11461 Saudi Arabia;
King Faisal Specialist Hosp &
Res Ctr Dept Genet Riyadh Saudi Arabia;
King Faisal Specialist Hosp &
Res Ctr Dept Genet Riyadh Saudi Arabia;
King Faisal Specialist Hosp &
Res Ctr Dept Genet Riyadh Saudi Arabia;
King Faisal Specialist Hosp &
Res Ctr Dept Genet Riyadh Saudi Arabia;
King Fahad Med City Womens Specialist Hosp Dept Maternal Fetal Med Riyadh Saudi Arabia;
King Fahad Med City Womens Specialist Hosp Dept Maternal Fetal Med Riyadh Saudi Arabia;
King Fahad Med City Womens Specialist Hosp Dept Maternal Fetal Med Riyadh Saudi Arabia;
King Fahad Med City Womens Specialist Hosp Dept Maternal Fetal Med Riyadh Saudi Arabia;
Cincinnati Childrens Hosp Med Ctr Div Human Genet Cincinnati OH 45229 USA;
Cincinnati Childrens Hosp Med Ctr Div Human Genet Cincinnati OH 45229 USA;
Hosp Sick Children Dept Paediat Div Clin &
Metab Genet Toronto ON Canada;
Hosp Sick Children Dept Paediat Div Clin &
Metab Genet Toronto ON Canada;
Hosp Sick Children Dept Paediat Div Clin &
Metab Genet Toronto ON Canada;
Hosp Sick Children Dept Paediat Div Clin &
Metab Genet Toronto ON Canada;
King Fahad Med City Childrens Hosp Dept Pediat Subspecialties Riyadh Saudi Arabia;
King Faisal Specialist Hosp &
Res Ctr Dept Genet Riyadh Saudi Arabia;
机译:家族性先天性脑积水的遗传景观
机译:家族性先天性脑积水的遗传景观
机译:家族性先天性脑积水的遗传景观
机译:家族肥厚性心肌病的遗传筛查
机译:两种家族性先天性心脏缺陷的病理和遗传特征。
机译:脑积水先天性脑积水。动物模型:牛脑积水先天性内部脑积水导水管狭窄。
机译:SLC12A离子转运蛋白突变在散发性和家族性人体先天性脑积水中