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Ser217Cys mutation in the Ig Ⅱ domain of FGFR3 in a Chinese family with autosomal dominant achondroplasia 被引量:9
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作者 ZHANG Shi-rong ZHOU Xiao-qing +5 位作者 REN Xiang WANG Tian-tian YUAN Ming-xiong WANG Qing LIU Jing-yu LIU Mu-gen 《Chinese Medical Journal》 SCIE CAS CSCD 2007年第11期1017-1019,共3页
Achondroplasia (ACH) is the most common form of skeletal dysplasia characterized by disproportionately short stature, lumbar lordosis, relative macrocephaly and other skeletal anomalies resulting from a defect in th... Achondroplasia (ACH) is the most common form of skeletal dysplasia characterized by disproportionately short stature, lumbar lordosis, relative macrocephaly and other skeletal anomalies resulting from a defect in the maturation of the chondrocytes in the growth plate of the cartilage. The combined frequency of the disease has been estimated to be 1 in 15 000 live births.1 ACH is inherited in autosomal dominant fashion with a complete penetrance, more than 80% of affected individuals have de novo mutations associated with increased paternal age. 展开更多
关键词 fibroblast growth factor receptor 3 ACHONDROPLASIA mutation linkage analysis
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