He R - Search Results

1

Evaluation of non-invasive prenatal testing to detect chromosomal aberrations in a Chinese cohort.

Cui W, Liu X, Zhang Y, Wang Y, Chu G, He R, Zhao Y. Cui W, et al. Among authors: he r. J Cell Mol Med. 2019 Nov;23(11):7873-7878. doi: 10.1111/jcmm.14614. Epub 2019 Aug 27. J Cell Mol Med. 2019. PMID: 31454164 Free PMC article.

2

[Chromosomal abnormality diagnosis of male infertility by QF-PCR].

Qi ML, Zhang YY, Liu XL, He R, Zhao YY. Qi ML, et al. Among authors: he r. Yi Chuan. 2011 Aug;33(8):895-900. doi: 10.3724/sp.j.1005.2011.00895. Yi Chuan. 2011. PMID: 21831806 Chinese.

3

Identification of immediate early gene X-1 as a cellular target gene of hcmv-mir-UL148D.

Wang YP, Qi Y, Huang YJ, Qi ML, Ma YP, He R, Ji YH, Sun ZR, Ruan Q. Wang YP, et al. Among authors: he r. Int J Mol Med. 2013 Apr;31(4):959-66. doi: 10.3892/ijmm.2013.1271. Epub 2013 Feb 6. Int J Mol Med. 2013. PMID: 23403649

4

[Genetic diagnosis of Duchenne/Becker muscular dystrophy by MLPA].

Zhang Y, Liu X, He R, Ma H, Zhao Y. Zhang Y, et al. Among authors: he r. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):338-43. doi: 10.3760/cma.j.issn.1003-9406.2014.03.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24928015 Chinese.

5

A new mutation in the gene ROR2 causes brachydactyly type B1.

Huang D, Jiang S, Zhang Y, Liu X, Zhang J, He R. Huang D, et al. Among authors: he r. Gene. 2014 Aug 15;547(1):106-10. doi: 10.1016/j.gene.2014.06.035. Epub 2014 Jun 19. Gene. 2014. PMID: 24954533

6

R75Q de novo dominant mutation of GJB2 in a Chinese family with hearing loss and palmoplantar keratoderma.

Jiang SJ, Di ZH, Huang D, Zhang JB, Zhang YY, Li SQ, He R. Jiang SJ, et al. Among authors: he r. Int J Pediatr Otorhinolaryngol. 2014 Sep;78(9):1461-6. doi: 10.1016/j.ijporl.2014.06.008. Epub 2014 Jun 16. Int J Pediatr Otorhinolaryngol. 2014. PMID: 24975403

7

A microdeletion of chromosome 9q33.3 encompasses the entire LMX1B gene in a Chinese family with nail patella syndrome.

Jiang S, Zhang J, Huang D, Zhang Y, Liu X, Wang Y, He R, Zhao Y. Jiang S, et al. Among authors: he r. Int J Mol Sci. 2014 Nov 5;15(11):20158-68. doi: 10.3390/ijms151120158. Int J Mol Sci. 2014. PMID: 25380522 Free PMC article.

8

[Application of quantitative fluorescence PCR for the prenatal diagnosis of common fetal chromosomal aneuploidies].

Liu X, Zhang Y, Cui W, He R, Zhao Y. Liu X, et al. Among authors: he r. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Oct;32(5):635-40. doi: 10.3760/cma.j.issn.1003-9406.2015.05.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26418981 Chinese.

9

Decreased Amino Acid Concentrations are Involved in Congenital Heart Disease.

Lai G, Li X, Zhang B, Wang L, He R, Zhao Y. Lai G, et al. Among authors: he r. Ann Nutr Metab. 2019;74(3):257-263. doi: 10.1159/000499405. Epub 2019 Mar 27. Ann Nutr Metab. 2019. PMID: 30917366

10

Keratin 9 L164P mutation in a Chinese pedigree with epidermolytic palmoplantar keratoderma, cytokeratin analysis, and literature review.

Liu X, Qiu C, He R, Zhang Y, Zhao Y. Liu X, et al. Among authors: he r. Mol Genet Genomic Med. 2019 Nov;7(11):e977. doi: 10.1002/mgg3.977. Epub 2019 Sep 16. Mol Genet Genomic Med. 2019. PMID: 31525823 Free PMC article. Review.

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