132 related articles for article (PubMed ID: 27228077)
1. Implementation of a High-Resolution Single-Nucleotide Polymorphism Array in Analyzing the Products of Conception.
Zhang H; Liu W; Chen M; Li Z; Sun X; Wang C
Genet Test Mol Biomarkers; 2016 Jul; 20(7):352-8. PubMed ID: 27228077
[TBL] [Abstract][Full Text] [Related]
2. Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis.
Levy B; Sigurjonsson S; Pettersen B; Maisenbacher MK; Hall MP; Demko Z; Lathi RB; Tao R; Aggarwal V; Rabinowitz M
Obstet Gynecol; 2014 Aug; 124(2 Pt 1):202-209. PubMed ID: 25004334
[TBL] [Abstract][Full Text] [Related]
3. Improved assay performance of single nucleotide polymorphism array over conventional karyotyping in analyzing products of conception.
Lin SB; Xie YJ; Chen Z; Zhou Y; Wu JZ; Zhang ZQ; Shi SS; Chen BJ; Fang Q
J Chin Med Assoc; 2015 Jul; 78(7):408-13. PubMed ID: 26004737
[TBL] [Abstract][Full Text] [Related]
4. Diagnostic utility of microarray testing in pregnancy loss.
Rosenfeld JA; Tucker ME; Escobar LF; Neill NJ; Torchia BS; McDaniel LD; Schultz RA; Chong K; Chitayat D
Ultrasound Obstet Gynecol; 2015 Oct; 46(4):478-86. PubMed ID: 25846569
[TBL] [Abstract][Full Text] [Related]
5. [Single nucleotide polymorphism-array in genetic analysis of chorionic villi from early spontaneous miscarriages].
Sun Y; Luo Y; Qian Y; Dong M; Jin F
Zhejiang Da Xue Xue Bao Yi Xue Ban; 2017 May; 46(3):262-267. PubMed ID: 29039167
[TBL] [Abstract][Full Text] [Related]
6. Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalities.
Mason-Suares H; Kim W; Grimmett L; Williams ES; Horner VL; Kunig D; Goldlust IS; Wu BL; Shen Y; Miller DT; Martin CL; Rudd MK
Genet Med; 2013 Sep; 15(9):706-12. PubMed ID: 23558256
[TBL] [Abstract][Full Text] [Related]
7. Single-Nucleotide Polymorphism-Microarray Ploidy Analysis of Paraffin-Embedded Products of Conception in Recurrent Pregnancy Loss Evaluations.
Maslow BS; Budinetz T; Sueldo C; Anspach E; Engmann L; Benadiva C; Nulsen JC
Obstet Gynecol; 2015 Jul; 126(1):175-81. PubMed ID: 26241271
[TBL] [Abstract][Full Text] [Related]
8. Clinical application of SNP array analysis in first-trimester pregnancy loss: a prospective study.
Wang Y; Cheng Q; Meng L; Luo C; Hu H; Zhang J; Cheng J; Xu T; Jiang T; Liang D; Hu P; Xu Z
Clin Genet; 2017 Jun; 91(6):849-858. PubMed ID: 27883173
[TBL] [Abstract][Full Text] [Related]
9. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
Kloth JN; Oosting J; van Wezel T; Szuhai K; Knijnenburg J; Gorter A; Kenter GG; Fleuren GJ; Jordanova ES
BMC Genomics; 2007 Feb; 8():53. PubMed ID: 17311676
[TBL] [Abstract][Full Text] [Related]
10. Clinical utilization of chromosomal microarray analysis for the genetic analysis in subgroups of pregnancy loss.
Gou L; Liu T; Wang Y; Wu Q; Hu S; Dong B; Wang C; Zhang Y; Shan X; Wang X; Suo F; Gu M
J Matern Fetal Neonatal Med; 2022 Nov; 35(22):4404-4411. PubMed ID: 33228446
[TBL] [Abstract][Full Text] [Related]
11. Cancer Sample Analysis Utilizing Single-Nucleotide Polymorphism Array and Array Comparative Genomic Hybridization.
Kang B; Xiao H; Ackley T; Shao L
Methods Mol Biol; 2024; 2825():151-171. PubMed ID: 38913308
[TBL] [Abstract][Full Text] [Related]
12. SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
D'Amours G; Langlois M; Mathonnet G; Fetni R; Nizard S; Srour M; Tihy F; Phillips MS; Michaud JL; Lemyre E
BMC Med Genomics; 2014 Dec; 7():70. PubMed ID: 25539807
[TBL] [Abstract][Full Text] [Related]
13. 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; 23():5550-5557. PubMed ID: 29162795
[TBL] [Abstract][Full Text] [Related]
14. Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays.
Treff NR; Su J; Tao X; Levy B; Scott RT
Fertil Steril; 2010 Nov; 94(6):2017-21. PubMed ID: 20188357
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Benefits and burdens of using a SNP array in pregnancies at increased risk for the common aneuploidies.
Van Opstal D; de Vries F; Govaerts L; Boter M; Lont D; van Veen S; Joosten M; Diderich K; Galjaard RJ; Srebniak MI
Hum Mutat; 2015 Mar; 36(3):319-26. PubMed ID: 25504762
[TBL] [Abstract][Full Text] [Related]
17. [Application of whole-genome and high-resolution chromosome microarray analysis for the investigation of fetuses with ultrasound abnormalities].
Zhang Y; Fu F; Li R; Xie G; Han J; Pan M; Zhen L; Yang X; Li D; Liao C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):169-74. PubMed ID: 25863078
[TBL] [Abstract][Full Text] [Related]
18. High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings.
Tyreman M; Abbott KM; Willatt LR; Nash R; Lees C; Whittaker J; Simonic I
J Med Genet; 2009 Aug; 46(8):531-41. PubMed ID: 19451135
[TBL] [Abstract][Full Text] [Related]
19. Allelic imbalance analysis by high-density single-nucleotide polymorphic allele (SNP) array with whole genome amplified DNA.
Wong KK; Tsang YT; Shen J; Cheng RS; Chang YM; Man TK; Lau CC
Nucleic Acids Res; 2004 May; 32(9):e69. PubMed ID: 15148342
[TBL] [Abstract][Full Text] [Related]
20. Single nucleotide polymorphism array analysis of cancer.
Dutt A; Beroukhim R
Curr Opin Oncol; 2007 Jan; 19(1):43-9. PubMed ID: 17133111
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]