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Effect of MSX1 on the cellular function of cardiomyocytes.
Gene. 2024 Jul 20;916:148419. doi: 10.1016/j.gene.2024.148419. Epub 2024 Mar 29.
Gene. 2024.
PMID: 38556116
Free article.
Prenatal diagnosis of pure partial monosomy 18p associated with holoprosencephaly and congenital heart defects.
Yi Z, Yingjun X, Yongzhen C, Liangying Z, Meijiao S, Baojiang C.
Yi Z, et al. Among authors: liangying z.
Gene. 2014 Jan 10;533(2):565-9. doi: 10.1016/j.gene.2013.09.027. Epub 2013 Oct 1.
Gene. 2014.
PMID: 24091065
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Copy number variations independently induce autism spectrum disorder.
Yingjun X, Haiming Y, Mingbang W, Liangying Z, Jiaxiu Z, Bing S, Qibin Y, Xiaofang S.
Yingjun X, et al. Among authors: liangying z.
Biosci Rep. 2017 Jul 7;37(4):BSR20160570. doi: 10.1042/BSR20160570. Print 2017 Aug 31.
Biosci Rep. 2017.
PMID: 28533427
Free PMC article.
Clinical Trial.
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Prader-Willi syndrome with a long-contiguous stretch of homozygosity not covering the critical region.
Yingjun X, Yi Z, Jianzhu W, Yunxia S, Yongzhen C, Liangying Z, Xiangyi J, Qun F.
Yingjun X, et al. Among authors: liangying z.
J Child Neurol. 2015 Mar;30(3):371-7. doi: 10.1177/0883073814535492. Epub 2014 May 22.
J Child Neurol. 2015.
PMID: 24859787
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