Mao J - 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: mao j. 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

A novel mutation of GATA4 in a familial atrial septal defect.

Chen Y, Mao J, Sun Y, Zhang Q, Cheng HB, Yan WH, Choy KW, Li H. Chen Y, et al. Among authors: mao j. Clin Chim Acta. 2010 Nov 11;411(21-22):1741-5. doi: 10.1016/j.cca.2010.07.021. Epub 2010 Jul 24. Clin Chim Acta. 2010. PMID: 20659440

3

[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: mao j. 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.

4

[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: mao j. Zhonghua Er Ke Za Zhi. 2011 Apr;49(4):316-9. Zhonghua Er Ke Za Zhi. 2011. PMID: 21624212 Chinese.

5

[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: mao j. 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.

6

[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. Among authors: mao j. 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.

7

[SLC26A4 mutations in a Chinese deafness family discovered by next-generation sequencing technology].

Mao J, Wei XM, Li H, Wang SN, Chen Y. Mao J, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Nov;47(11):942-5. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 23302201 Chinese.

8

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. Among authors: mao j. 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.

9

Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy.

Mao J, Wang T, Wang BJ, Liu YH, Li H, Zhang J, Cram D, Chen Y. Mao J, et al. Clin Chim Acta. 2014 Jun 10;433:190-3. doi: 10.1016/j.cca.2014.03.011. Epub 2014 Mar 22. Clin Chim Acta. 2014. PMID: 24667696

10

[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. Among authors: mao j. 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.

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