198 related articles for article (PubMed ID: 37916154)
1. Analysis of copy number variations and possible candidate genes in spontaneous abortion by copy number variation sequencing.
Bai W; Zhang Q; Lin Z; Ye J; Shen X; Zhou L; Cai W
Front Endocrinol (Lausanne); 2023; 14():1218793. PubMed ID: 37916154
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 25767059
[TBL] [Abstract][Full Text] [Related]
3. Sequential application of copy number variation sequencing and quantitative fluorescence polymerase chain reaction in genetic analysis of miscarriage and stillbirth.
Chen Q; Zhang H; Li X; Li J; Chen H; Liu L; Zhou S; Xu Z
Mol Genet Genomic Med; 2023 Aug; 11(8):e2187. PubMed ID: 37073418
[TBL] [Abstract][Full Text] [Related]
4. Copy number variation characterization and possible candidate genes in miscarriage and stillbirth by next-generation sequencing analysis.
Zhang X; Huang Q; Yu Z; Wu H
J Gene Med; 2021 Dec; 23(12):e3383. PubMed ID: 34342101
[TBL] [Abstract][Full Text] [Related]
5. Systematic analysis of copy-number variations associated with early pregnancy loss.
Wang Y; Li Y; Chen Y; Zhou R; Sang Z; Meng L; Tan J; Qiao F; Bao Q; Luo D; Peng C; Wang YS; Luo C; Hu P; Xu Z
Ultrasound Obstet Gynecol; 2020 Jan; 55(1):96-104. PubMed ID: 31364215
[TBL] [Abstract][Full Text] [Related]
6. Experience of copy number variation sequencing applied in spontaneous abortion.
Dai YF; Wu XQ; Huang HL; He SQ; Guo DH; Li Y; Lin N; Xu LP
BMC Med Genomics; 2024 Jan; 17(1):15. PubMed ID: 38191380
[TBL] [Abstract][Full Text] [Related]
7. A pilot investigation of low-pass genome sequencing identifying site-specific variation in chromosomal mosaicisms by a multiple site sampling approach in first-trimester miscarriages.
Li Y; Chau MHK; Zhang YX; Zhao Y; Xue S; Li TC; Cao Y; Dong Z; Choy KW; Chung JPW
Hum Reprod; 2023 Aug; 38(8):1628-1642. PubMed ID: 37218343
[TBL] [Abstract][Full Text] [Related]
8. Chromosomal Copy Number Variation Analysis in Pregnancy Products from Recurrent and Sporadic Miscarriage Using Next-Generation Sequencing.
Zhang X; Wu H; Gu Z; Yu Z; Lan L; Huang Q
Reprod Sci; 2022 Oct; 29(10):2927-2936. PubMed ID: 35578104
[TBL] [Abstract][Full Text] [Related]
9. The chromosomal characteristics of spontaneous abortion and its potential associated copy number variants and genes.
Qin Y; Touch K; Sha M; Sun Y; Zhang S; Wu J; Wu Y; Feng L; Chen S; Xiao J
J Assist Reprod Genet; 2024 May; 41(5):1285-1296. PubMed ID: 38668959
[TBL] [Abstract][Full Text] [Related]
10. Characterization of Copy-Number Variations and Possible Candidate Genes in Recurrent Pregnancy Losses.
Sheng YR; Hou SY; Hu WT; Wei CY; Liu YK; Liu YY; Jiang L; Xiang JJ; Sun XX; Lei CX; Wang HL; Zhu XY
Genes (Basel); 2021 Jan; 12(2):. PubMed ID: 33499090
[TBL] [Abstract][Full Text] [Related]
11. Copy number variation sequencing combined with quantitative fluorescence polymerase chain reaction in clinical application of pregnancy loss.
Chen L; Wang L; Tang F; Zeng Y; Yin D; Zhou C; Zhu H; Li L; Zhang L; Wang J
J Assist Reprod Genet; 2021 Sep; 38(9):2397-2404. PubMed ID: 34052955
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of 913 fetuses samples using copy number variation sequencing.
Lan L; She L; Zhang B; He Y; Zheng Z
J Gene Med; 2021 May; 23(5):e3324. PubMed ID: 33615614
[TBL] [Abstract][Full Text] [Related]
13. Maternal age, history of miscarriage, and embryonic/fetal size are associated with cytogenetic results of spontaneous early miscarriages.
Ozawa N; Ogawa K; Sasaki A; Mitsui M; Wada S; Sago H
J Assist Reprod Genet; 2019 Apr; 36(4):749-757. PubMed ID: 30739229
[TBL] [Abstract][Full Text] [Related]
14. Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with congenital gastrointestinal obstruction.
Meng X; Jiang L
BMC Pregnancy Childbirth; 2022 Jan; 22(1):50. PubMed ID: 35045821
[TBL] [Abstract][Full Text] [Related]
15. Potential genetic causes of miscarriage in euploid pregnancies: a systematic review.
Colley E; Hamilton S; Smith P; Morgan NV; Coomarasamy A; Allen S
Hum Reprod Update; 2019 Jul; 25(4):452-472. PubMed ID: 31150545
[TBL] [Abstract][Full Text] [Related]
16. 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. PubMed ID: 30732499
[TBL] [Abstract][Full Text] [Related]
17. Cytogenetic and genetic investigation of miscarriage cases in Eastern China.
Wang H; Yuan D; Wang S; Luo L; Zhang Y; Ye J; Zhu K
J Matern Fetal Neonatal Med; 2020 Oct; 33(20):3385-3390. PubMed ID: 30741046
[No Abstract] [Full Text] [Related]
18. [Chorionic villus cell culture and karyotype analysis in 1 983 cases of spontaneous miscarriage].
Yuan SM; Liao C; Li DZ; Huang JZ; Hu SY; Ke M; Zhong HZ; Yi CX
Zhonghua Fu Chan Ke Za Zhi; 2017 Jul; 52(7):461-466. PubMed ID: 28797153
[No Abstract] [Full Text] [Related]
19. Analysis of copy number variation by sequencing in fetuses with nuchal translucency thickening.
Lan L; Wu H; She L; Zhang B; He Y; Luo D; Wang H; Zheng Z
J Clin Lab Anal; 2020 Aug; 34(8):e23347. PubMed ID: 32342531
[TBL] [Abstract][Full Text] [Related]
20. Study on the correlation between the ultrasound phenotype and copy number variation of abnormal embryo in spontaneous abortion.
Tan S; Pan P; Yang Z; Su J; Wei H
J Obstet Gynaecol Res; 2021 Nov; 47(11):3779-3788. PubMed ID: 34571575
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
