Ge Y - Search Results

1

Newborn Screening for G6PD Deficiency in Xiamen, China: Prevalence, Variant Spectrum, and Genotype-Phenotype Correlations.

Wang X, Xia Z, He Y, Zhou X, Zhang H, Gao C, Ge Y, Cai X, Zhou Y, Guo Q. Wang X, et al. Among authors: ge y. Front Genet. 2021 Oct 1;12:718503. doi: 10.3389/fgene.2021.718503. eCollection 2021. Front Genet. 2021. PMID: 34659341 Free PMC article.

2

[Molecular cytogenetic studies of 25 males with azoospermia].

Ge YS, Zhou YL, Wu HN. Ge YS, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Apr;25(2):190-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18393244 Chinese.

3

[Application of fluorescence in situ hybridization in prenatal diagnosis of complex chromosomal abnormalities].

Shen YY, Li J, Kong H, Wu HN, Wu Q, Ge YS, Huang XL, Zhou YL. Shen YY, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):529-32. doi: 10.3760/cma.j.issn.1003-9406.2009.05.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19806574 Chinese.

4

[Genetic counseling and clinical outcome of fetus with de novo chromosomal aberrations].

Wu QC, Kong H, Sun L, Wang WB, Ge YS, Xu YS, Zhou YL. Wu QC, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Feb;28(1):56-9. doi: 10.3760/cma.j.issn.1003-9406.2011.01.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21287511 Chinese.

5

Investigation of the frequencies of prenatally diagnosed fetal chromosomal abnormalities at a single institution.

Wu Q, Wang W, Kong H, Sun L, Ge Y, Xu Y, Zhou Y. Wu Q, et al. Among authors: ge y. Fetal Pediatr Pathol. 2013 Jun;32(3):163-8. doi: 10.3109/15513815.2012.684847. Epub 2012 May 18. Fetal Pediatr Pathol. 2013. PMID: 22607389

6

Rapid and simultaneous screening of 47,XXY and AZF microdeletions by quadruplex real-time polymerase chain reaction.

Zhou Y, Ge Y, Xiao L, Guo Q. Zhou Y, et al. Among authors: ge y. Reprod Biol. 2015 Jun;15(2):113-21. doi: 10.1016/j.repbio.2015.02.002. Epub 2015 Feb 20. Reprod Biol. 2015. PMID: 26051460

7

Diagnosis of a Chinese man with 45,X/46,X,i(Y)(q10)/47,X,i(Y) (q10) ×2 mosaic Turner syndrome.

Sha YW, Ding L, Ji ZY, Ge YS, Kong H, Zhang Q, Zhou YL, Li P. Sha YW, et al. Asian J Androl. 2018 Mar-Apr;20(2):205-207. doi: 10.4103/1008-682X.193162. Asian J Androl. 2018. PMID: 28091398 Free PMC article. No abstract available.

8

Carrier screening for spinal muscular atrophy with a simple test based on melting analysis.

Xia Z, Zhou Y, Fu D, Wang Z, Ge Y, Ren J, Guo Q. Xia Z, et al. Among authors: ge y. J Hum Genet. 2019 May;64(5):387-396. doi: 10.1038/s10038-019-0576-6. Epub 2019 Feb 15. J Hum Genet. 2019. PMID: 30765868

9

[Prenatal diagnosis of a fetus with two small supernumerary marker chromosomes].

Zhang J, Jiang Y, Cai M, Ge Y, Zhou Y, Wang W. Zhang J, et al. Among authors: ge y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Dec 10;36(12):1222-1225. doi: 10.3760/cma.j.issn.1003-9406.2019.12.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31813153 Chinese.

10

[Prenatal genetic analysis of three fetuses with abnormalities of chromosome 22].

Ge Y, Zhang J, Cai M, Chen X, Zhou Y. Ge Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Apr 10;37(4):405-409. doi: 10.3760/cma.j.issn.1003-9406.2020.04.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32219823 Chinese.

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