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Shunyao Liao
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Shunyao Liao
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Shunyao Liao
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1
Novel compound heterozygous mutations of ALDH1A3 contribute to anophthalmia in a non-consanguineous Chinese family
by
Yunqiang Liu
,
Yongjie Lu
,
Shasha Liu
,
Shunyao
Liao
Published 2017-06-01
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Article
2
Whole-exome sequencing of de novo genetic variants in a Chinese family with a sporadic case of congenital nonsyndromic hearing loss [version 2; peer review: 2 approved]
by
Sijing Hu
,
Hao Zhang
,
Yunqiang Liu
,
Mohan Liu
,
Jingjing Li
,
Shunyao
Liao
Published 2021-08-01
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Article
3
Association of genetic variants of melatonin receptor 1B with gestational plasma glucose level and risk of glucose intolerance in pregnant Chinese women.
by
Shunyao
Liao
,
Yunqiang Liu
,
Yuande Tan
,
Lu Gan
,
Jie Mei
,
Wenzhong Song
,
Shu Chi
,
Xianjue Dong
,
Xiaojuan Chen
,
Shaoping Deng
Published 2012-01-01
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