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Items: 1 to 20 of 104

1.

[Identification of cryptic structural chromosomal aberrations in parents through detection of copy number variations in miscarriage tissues].

Zhao Y, Pang H, Guo S, Cheng Z, Sun J, Lan C, Zhao Y, Sun R, Zhang M, Fan T, Yan X.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Nov 10;36(11):1123-1126. doi: 10.3760/cma.j.issn.1003-9406.2019.11.017. Chinese.

PMID:
31703141
2.

Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage.

Liu S, Song L, Cram DS, Xiong L, Wang K, Wu R, Liu J, Deng K, Jia B, Zhong M, Yang F.

Ultrasound Obstet Gynecol. 2015 Oct;46(4):472-7. doi: 10.1002/uog.14849.

3.

[Application of next generation sequencing for the analysis of patients with spontaneous abortion].

Zhang J, Xie J, Jiang S, Zhang J, Yang Y, Wang S, Wu X, Chen C, Yao F, Zhang Y.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):835-838. doi: 10.3760/cma.j.issn.1003-9406.2017.06.011. Chinese.

PMID:
29188611
4.

[Genetic diagnosis and noninvasive prenatal testing of a family with Williams-Beuren syndrome].

Zhao Y, Pang H, Feng X, Xiang Y, Gao M, Hua J, Tong D, Wu L, Sun H.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):263-266. doi: 10.3760/cma.j.issn.1003-9406.2019.03.018. Chinese.

PMID:
30835361
5.

Prevalence of chromosomal abnormalities identified by copy number variation sequencing in high-risk pregnancies, spontaneous abortions, and suspected genetic disorders.

Zhang R, Chen X, Wang D, Chen X, Wang C, Zhang Y, Xu M, Yu J.

J Int Med Res. 2019 Mar;47(3):1169-1178. doi: 10.1177/0300060518818020. Epub 2019 Feb 7.

6.

[Application of next generation sequencing for the detection of chromosomal aneuploidies and copy number variations in abortus tissues].

Chen J, Hu L, Yang J, Liu P.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):591-594. doi: 10.3760/cma.j.issn.1003-9406.2018.04.029. Chinese.

PMID:
30098263
7.

[Application of chromosomal microarray analysis and next-generation sequencing for the analysis of abortic tissues].

Zhao W, Li S, Miao Y, Li J, Yu D.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):676-681. doi: 10.3760/cma.j.issn.1003-9406.2019.07.005. Chinese.

PMID:
31302909
8.

Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.

Qu S, Wang L, Cai A, Cui S, Bai N, Liu N, Kong X.

J Matern Fetal Neonatal Med. 2019 Jan;32(1):1-10. doi: 10.1080/14767058.2017.1367379. Epub 2017 Oct 16.

PMID:
29034762
9.

Clinical application of whole-genome low-coverage next-generation sequencing to detect and characterize balanced chromosomal translocations.

Liang D, Wang Y, Ji X, Hu H, Zhang J, Meng L, Lin Y, Ma D, Jiang T, Jiang H, Asan, Song L, Guo J, Hu P, Xu Z.

Clin Genet. 2017 Apr;91(4):605-610. doi: 10.1111/cge.12844. Epub 2016 Sep 5.

PMID:
27491356
10.

Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypes.

Gijsbers AC, Bosch CA, Dauwerse JG, Giromus O, Hansson K, Hilhorst-Hofstee Y, Kriek M, van Haeringen A, Bijlsma EK, Bakker E, Breuning MH, Ruivenkamp CA.

Eur J Med Genet. 2010 Sep-Oct;53(5):227-33. doi: 10.1016/j.ejmg.2010.06.003. Epub 2010 Jun 11.

PMID:
20542150
11.

[Application of array-based comparative genomic hybridization technique in genetic analysis of patients with spontaneous abortion].

Chu Y, Wu D, Hou QF, Huo XD, Gao Y, Wang T, Wang HD, Yang YL, Liao SX.

Zhonghua Fu Chan Ke Za Zhi. 2016 Aug 25;51(8):592-6. doi: 10.3760/cma.j.issn.0529-567X.2016.08.008. Chinese.

PMID:
27561938
12.

[Detection for chromosomal aberrations in 43 fetuses with spontaneous abortion and stillbirth by array-based comparative genomic hybridization].

Li Y, Gong Y, Liu H, Song Y, He W, Wei J, Sun X, Chen X.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Jun;32(3):348-52. doi: 10.3760/cma.j.issn.1003-9406.2015.03.010. Chinese.

PMID:
26037348
13.

[Cytogenetic study of 1780 cases of spontaneous abortion].

Qian WP, Tan YM, Song D, Tan YQ, Lu GX.

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2005 Jun;30(3):258-60. Chinese.

14.

[Identification of complex chromosomal aberrations in acute leukemia by using conventional cytogenetics combined with multiplex fluorescence in situ hybridization].

Yu F, Li CW, Wei H, Liu XP, Lin D, Gong JY, Qin S, Xu FY, Mi YC, Wang JX.

Zhonghua Xue Ye Xue Za Zhi. 2010 May;31(5):289-93. Chinese.

PMID:
21122305
15.

[Phenotypic and genetic analysis of a pedigree with 4p16 microduplication and 8p23 microdeletion].

Li C, Hou R, Liu C, Li LJ, Lyu Y.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Oct 10;36(10):989-992. doi: 10.3760/cma.j.issn.1003-9406.2019.10.009. Chinese.

PMID:
31598942
16.

[Analysis of genomic copy number variations in 36 fetuses with heart malformations using next-generation sequencing].

Gao M, Pang H, Zhao Y, Li-Ling J.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):524-527. doi: 10.3760/cma.j.issn.1003-9406.2017.04.012. Chinese.

PMID:
28777851
17.

Semiconductor Sequencing Analysis of Chromosomal Copy Number Variations in Spontaneous Miscarriage.

Wang MZ, Lin FQ, Li M, He D, Yu QH, Yang XX, Wu YS.

Med Sci Monit. 2017 Nov 22;23:5550-5557.

18.

[Application of chromosomal microarray analysis for a cohort of Chinese patients with spontaneous miscarriage].

Yuan H, Chen M, Deng X, Lyu F.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Aug;33(4):442-6. doi: 10.3760/cma.j.issn.1003-9406.2016.04.003. Chinese.

PMID:
27454994
19.

[Diagnosis of a case with recurrent pregnancy loss resulted from maternal balanced translocation by chromosomal microarray analysis].

Wang L, Bai N, Liu L, Zhang Q, Kong X.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Jun 10;35(3):443-447. doi: 10.3760/cma.j.issn.1003-9406.2018.03.032. Chinese.

PMID:
29896752
20.

[Application of copy number variation analysis based on next-generation sequencing in the genetic analysis of missed abortion chorionic villi].

Qi H, Cai LR, Zhu JJ, Yang K, Wen XH, Zeng W, Chen JL.

Zhonghua Fu Chan Ke Za Zhi. 2016 Feb;51(2):92-7. doi: 10.3760/cma.j.issn.0529-567X.2016.02.003. Chinese.

PMID:
26917476

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