英语词汇“polydactyly”的意思、用法、释义、翻译、读音、例句、短语、词组-英语词典

是什么意思

释义

多指[畸形]，多趾[畸形]；

英英释义

polydactyly

n.birth defect characterized by the presence of more than the normal number of fingers or toes
同义词：hyperdactyly

学习怎么用

权威例句

Polydactyly and ectopic ZPA formation in Alx-4 mutant mice
Mutation in GLI3 in postaxial polydactyly type A.
NEK1 mutations cause short-rib polydactyly syndrome type majewski.
Evidence that preaxial polydactyly in the Doublefoot mutant is due to ectopic Indian Hedgehog signaling.
Mutations in mouse Aristaless-like4 cause Strong's luxoid polydactyly.
Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly.
DYNC2H1 mutations cause asphyxiating thoracic dystrophy and short rib-polydactyly syndrome, type III
A Syndrome Characterized by Ectodermal Dysplasia, Polydactyly, Chondro-Dysplasia and Congenital Morbus Cordis: Report of Three Cases
Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome
The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly typ...

单词	polydactyly
释义	polydactyly 听听怎么读英 [p??'l?d?kt?l?] 美 [po?'l?d?kt?l?] 是什么意思释义多指[畸形]，多趾[畸形]；英英释义 polydactyly n.birth defect characterized by the presence of more than the normal number of fingers or toes 同义词：hyperdactyly 学习怎么用权威例句 Polydactyly and ectopic ZPA formation in Alx-4 mutant mice Mutation in GLI3 in postaxial polydactyly type A. NEK1 mutations cause short-rib polydactyly syndrome type majewski. Evidence that preaxial polydactyly in the Doublefoot mutant is due to ectopic Indian Hedgehog signaling. Mutations in mouse Aristaless-like4 cause Strong's luxoid polydactyly. Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly. DYNC2H1 mutations cause asphyxiating thoracic dystrophy and short rib-polydactyly syndrome, type III A Syndrome Characterized by Ectodermal Dysplasia, Polydactyly, Chondro-Dysplasia and Congenital Morbus Cordis: Report of Three Cases Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly typ...
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