英语词汇“zori”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

（日本的）草鞋，便鞋；

变形

复数：zoris

英英释义

zori[ 'z?uri ]

n.a sandal attached to the foot by a thong over the toes
同义词：pusher

学习怎么用

双语例句

用作名词(n.)

In time, people began wearing zori for farm work.
后来,人们在田间作业时也开始普遍地穿草屐。

权威例句

Real-time language independent lip synchronization method using a genetic algorithm
Distinct phenotypes distinguish the molecular classes of Angelman syndrome
Aldehyde dehydrogenase activity as a functional marker for lung cancer
Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.
A DNA methylation imprint, determined by the sex of the parent, distinguishes the angelman and Prader-Willi syndromes ☆
TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome
Unexpected death and critical illness in Prader-Willi syndrome: report of ten individuals
A family with a grand-maternally derived interstitial duplication of proximal 15q.
Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.
Genetic insights into familial cancers – update and recent discoveries

单词	zori
释义	zori 听听怎么读英 ['z??r?] 美 ['zo?r?] 是什么意思 n. （日本的）草鞋，便鞋；变形复数：zoris 英英释义 zori[ 'z?uri ] n.a sandal attached to the foot by a thong over the toes 同义词：pusher 学习怎么用双语例句用作名词(n.) In time, people began wearing zori for farm work. 后来,人们在田间作业时也开始普遍地穿草屐。权威例句 Real-time language independent lip synchronization method using a genetic algorithm Distinct phenotypes distinguish the molecular classes of Angelman syndrome Aldehyde dehydrogenase activity as a functional marker for lung cancer Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting. A DNA methylation imprint, determined by the sex of the parent, distinguishes the angelman and Prader-Willi syndromes ☆ TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome Unexpected death and critical illness in Prader-Willi syndrome: report of ten individuals A family with a grand-maternally derived interstitial duplication of proximal 15q. Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia. Genetic insights into familial cancers – update and recent discoveries
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