Liu MJ - Search Results

1

A patient with five chromosomal rearrangements and a 2q31.1 microdeletion.

Wang T, Mao J, Liu MJ, Choy KW, Li HB, Cram DS, Li H, Chen Y. Wang T, et al. Among authors: liu mj. Clin Chim Acta. 2014 Mar 20;430:129-33. doi: 10.1016/j.cca.2014.01.002. Epub 2014 Jan 9. Clin Chim Acta. 2014. PMID: 24412318

2

[22q11 microdeletion test in patients with congenital heart defects by quantitative fluorescent PCR].

Chen Y, Mao J, Kwok KY, Kan HJ, Cheng HB, Li HB, Liu MJ, Sun Y, Yan WH, Li H, Choy KW. Chen Y, et al. Among authors: liu mj. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Oct;27(5):571-5. doi: 10.3760/cma.j.issn.1003-9406.2010.05.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20931540 Chinese.

3

[Clinical detection of 22q11 microdeletion in the patients with congenital heart disease by multiplex ligation dependent probe amplification].

Chen Y, Kan HJ, Mao J, Ding J, Meng QX, Li HB, Cheng HB, Liu MJ, Sun Y, Yan WH, Li H. Chen Y, et al. Among authors: liu mj. Zhonghua Er Ke Za Zhi. 2011 Apr;49(4):316-9. Zhonghua Er Ke Za Zhi. 2011. PMID: 21624212 Chinese.

4

[Genetic screening of mutation hot-spots for nonsyndromic hearing loss in southern Jiangsu province with SNaPshot].

Li H, Li HB, Mao J, Liu MJ, Cheng HB, Li SL, Chen Y. Li H, et al. Among authors: liu mj. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Aug;28(4):383-6. doi: 10.3760/cma.j.issn.1003-9406.2011.04.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21811975 Chinese.

5

[Application of next-generation sequencing technology for genetic diagnosis of Duchenne muscular dystrophy].

Liu MJ, Xie M, Mao J, Li H, Yan WH, Chen Y. Liu MJ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Jun;29(3):249-54. doi: 10.3760/cma.j.issn.1003-9406.2012.03.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22678781 Chinese.

6

[Analysis of GJB2 gene and mitochondrial DNA A1555G mutations in 16 families with non-syndromic hearing loss].

Wang W, Cheng HB, Yang N, Shi YC, Liu JZ, Li Q, Yang SM, Shen LY, Liu MJ, Chen Y, Li H. Wang W, et al. Among authors: liu jz, liu mj. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):388-92. doi: 10.3760/cma.j.issn.1003-9406.2012.04.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875492 Chinese.

7

Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease.

Wang B, Liu M, Yan W, Mao J, Jiang D, Li H, Chen Y. Wang B, et al. J Matern Fetal Neonatal Med. 2013 Dec;26(18):1768-77. doi: 10.3109/14767058.2013.799648. Epub 2013 Jun 10. J Matern Fetal Neonatal Med. 2013. PMID: 23701284 Free article.

8

[A microdeletion of chromosome 9q34.11 may cause suspected cerebral palsy].

Li H, Chen Y, Li Q, Liu M, Mao J, Song D, Li H. Li H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):725-9. doi: 10.3760/cma.j.issn.1003-9406.2014.06.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449075 Chinese.

9

Detection of complex deletions in chromosomes 13 and 21 in a fetus by noninvasive prenatal testing.

Wang T, Duan C, Shen C, Xiang J, He Q, Ding J, Wen P, Zhang Q, Wang W, Liu M, Li H, Li H, Zhang L. Wang T, et al. Mol Cytogenet. 2016 Jan 12;9:3. doi: 10.1186/s13039-016-0213-4. eCollection 2016. Mol Cytogenet. 2016. PMID: 26759606 Free PMC article.

10

Methylenetetrahydrofolate reductase polymorphisms at 3'-untranslated region are associated with susceptibility to preterm birth.

Zhu Q, Chen Y, Dai J, Wang B, Liu M, Wang Y, Tao J, Li H. Zhu Q, et al. Transl Pediatr. 2015 Jan;4(1):57-62. doi: 10.3978/j.issn.2224-4336.2015.01.02. Transl Pediatr. 2015. PMID: 26835361 Free PMC article.

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