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1 n NEK1 as an underlying cause of this lethal osteochondrodysplasia.
2 these compound mutant mice develop a unique osteochondrodysplasia.
3 osteoarthritis (OA) with a wide spectrum of osteochondrodysplasia.
4 s, hydrops fetalis, spina bifida occulta and osteochondrodysplasia.
5 seal dysplasia, two human autosomal dominant osteochondrodysplasias.
6 (SMC) are similar, rare autosomal recessive osteochondrodysplasias.
10 Cort dysplasia is a rare autosomal recessive osteochondrodysplasia characterized by short limbs and a
12 ndromas in the long bones and the ubiquitous osteochondrodysplasia of vertebral bodies to the occasio
13 hypertrichosis, craniofacial dysmorphology, osteochondrodysplasia, patent ductus arteriosus, cardiom
14 is a relatively mild and clinically variable osteochondrodysplasia, primarily characterized by delaye
16 yseal dysplasia (MED) are autosomal dominant osteochondrodysplasias that result in mild to severe sho
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