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1 the COMP gene cause pseudoachondroplasia and multiple epiphyseal dysplasia.
2 the development of pseudoachondroplasia and multiple epiphyseal dysplasia.
3 in the etiology of pseudoachondroplasia and multiple epiphyseal dysplasia.
4 keletal dysplasias, pseudoachondroplasia and multiple epiphyseal dysplasia.
5 nically related chondrodysplasias, PSACH and multiple epiphyseal dysplasia.
6 otypes of inherited pseudoachondroplasia and multiple epiphyseal dysplasia.
7 splasias that include diastrophic dysplasia, multiple epiphyseal dysplasia, atelosteogenesis type 2 a
8 keletal dysplasias, pseudoachondroplasia and multiple epiphyseal dysplasia; both show a characteristi
9 keletal dysplasias, pseudoachondroplasia and multiple epiphyseal dysplasia, disturb COMP secretion le
10 ocytes from pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (EDM1) patients display an
12 the development of pseudoachondroplasia and multiple epiphyseal dysplasia; however, the functions of
13 Col9a2, Col9a3, Comp, and Matn3 genes cause multiple epiphyseal dysplasia, in which patients develop
14 secretory defect in pseudoachondroplasia and multiple epiphyseal dysplasia is not specific for chondr
15 ted, including spondyloepiphyseal dysplasia, multiple epiphyseal dysplasia, Legg-Calve-Perthes diseas
16 is region contains the genes responsible for multiple epiphyseal dysplasia (MED) and pseudoachondropl
25 type 2 or DTD, whereas the milder, recessive multiple epiphyseal dysplasia phenotype is homozygous fo
26 been identified in pseudoachondroplasia and multiple epiphyseal dysplasia, two human autosomal domin
27 nown to result in pseudoachondrodysplasia or multiple epiphyseal dysplasia when found in the homologo
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