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Best diagnostic approach for the genetic evaluation of fetuses after intrauterine death in first, second or third trimester: QF-PCR, karyotyping and/or genome wide SNP array analysis

机译：妊娠中期，中期或晚期子宫内胎儿遗传学评估的最佳诊断方法：QF-PCR，核型分析和/或全基因组SNP阵列分析

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Angelique JA Kooper; Brigitte HW Faas; Ilse Feenstra; Nicole de Leeuw; Dominique FCM Smeets;
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1. Best diagnostic approach for the genetic evaluation of fetuses after intrauterine death in first, second or third trimester: QF-PCR, karyotyping and/or genome wide SNP array analysis [J] . Angelique JA Kooper, Brigitte HW Faas, Ilse Feenstra, Molecular cytogenetics . 2014,第1期

机译：妊娠中期，中期或中期子宫内胎儿遗传学评估的最佳诊断方法：QF-PCR，核型分析和/或全基因组SNP阵列分析
2. Non-targeted whole genome 250K SNP array analysis as replacement for karyotyping in fetuses with structural ultrasound anomalies: Evaluation of a one-year experience [J] . FaasB.H., FeenstraI., EgginkA.J., Prenatal Diagnosis . 2012,第4期

机译：非靶向全基因组250K SNP阵列分析可替代结构性超声异常胎儿的核型分析：一年经验评估
3. QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first-trimester prenatal diagnoses [J] . Grati Francesca R., Malvestiti Francesca, Grimi Beatrice, Prenatal Diagnosis . 2013,第Null期

机译：QF-PCR替代绒毛膜细胞滋养细胞核型分析：绒毛膜绒毛分析：44,727例早孕产前诊断的细胞遗传学回顾性审核的优点和局限性
4. GPU-based genome-wide SNP-SNP interactions detection and pancreatic cancer susceptibility analysis [C] . Xiao Wang, Qinke Peng, Yue Fan, 2016 IEEE-EMBS Conference on Biomedical Engineering and Sciences . 2016

机译：基于GPU的全基因组SNP-SNP相互作用检测和胰腺癌易感性分析
5. Polygenic analysis of genome-wide SNP data [D] . Simonson, Matthew A. 2013

机译：全基因组SNP数据的多基因分析
6. Best diagnostic approach for the genetic evaluation of fetuses after intrauterine death in first second or third trimester: QF-PCR karyotyping and/or genome wide SNP array analysis [O] . Angelique JA Kooper, Brigitte HW Faas, Ilse Feenstra, 2014

机译：妊娠中期中期或晚期子宫内胎儿遗传学评估的最佳诊断方法：QF-PCR核型分析和/或全基因组SNP阵列分析
7. Best diagnostic approach for the genetic evaluation of fetuses after intrauterine death in first, second or third trimester: QF-PCR, karyotyping and/or genome wide SNP array analysis [O] . Kooper A.J.A., Faas B.H.W., Feenstra I., 2014

机译：妊娠中期，中期或中期子宫内胎儿遗传学评估的最佳诊断方法：QF-PCR，核型分析和/或全基因组SNP阵列分析
8. Genome-Wide Association Mapping for Intelligence in Military Working Dogs: Canine Cohort, Canine Intelligence Assessment Regimen, Genome-Wide Single Nucleotide Polymorphism (SNP) Typing, and Unsupervised Classification Algorithm for Genome-Wide Association Data Analysis [R] . Chan, V. T., Mauzy, C. A., Soto, A., 2011

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Best diagnostic approach for the genetic evaluation of fetuses after intrauterine death in first, second or third trimester: QF-PCR, karyotyping and/or genome wide SNP array analysis

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