Preselection of cases through expert clinical and radiological review significantly increases mutation detection rate in multiple epiphyseal dysplasia.
第一作者:
Andreas,Zankl
第一单位:
Division of Molecular Paediatrics, Lausanne, Switzerland.
作者:
主题词
成年人(Adult);儿童, 学龄前(Child, Preschool);DNA突变分析(DNA Mutational Analysis);细胞外基质蛋白质类(Extracellular Matrix Proteins);女(雌)性(Female);基因检测(Genetic Testing);糖蛋白类(Glycoproteins);人类(Humans);男(雄)性(Male);中年人(Middle Aged);突变(Mutation);骨软骨发育不良(Osteochondrodysplasias);放射摄影术(Radiography)
DOI
10.1038/sj.ejhg.5201744
PMID
17133256
发布时间
2018-11-13
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