机译:宫颈动脉扫描术在FBN1 FBN1-相关的Weill-Markesani综合征中扩张心血管表型
Cardiovascular Genetics ProgramMassachusetts General HospitalBoston Massachusetts;
Maine Medical PartnersGenetics DivisionPortland Maine;
Thoracic Aortic CenterMassachusetts General HospitalBoston Massachusetts;
Cardiology Department of MedicineMassachusetts General HospitalBoston Massachusetts;
Genetics Unit Massachusetts General HospitalHarvard Medical SchoolBoston Massachusetts;
Cardiovascular Genetics ProgramMassachusetts General HospitalBoston Massachusetts;
acromelic dysplasia; cervical artery dissection; thoracic aortic aneurysm; Weill–Marchesani syndrome;
机译:宫颈动脉扫描术在FBN1 FBN1-相关的Weill-Markesani综合征中扩张心血管表型
机译:用低渗透的FBN1突变引起的威尔 - Markesani样综合征
机译:具有外显子24-32的FBN1突变的早期发作形式的Marfan综合征患者的心血管表型严重程度不同
机译:Weill-Marchesans综合征的超声检查
机译:FBN1外显子41和42的错义突变导致Weill-Marchesani综合征合并胸主动脉疾病和Marfan综合征
机译:患有宫颈曲折动脉和皮质出血的Marfan综合症:FBN1基因内含子中突变的情况