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Noninvasive Prenatal Screening at Low Fetal Fraction: Comparing Whole-Genome Sequencing and Single-Nucleotide Polymorphism Methods

机译：低胎儿分数的非侵入性产前筛选：比较全基因组测序和单核苷酸多态性方法

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Carlo G. Artieri; Carrie Haverty; Eric A. Evans; James D. Goldberg; Imran S. Haque; Yuval Yaron; Dale Muzzey;
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年度 2016
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1. Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods [J] . Artieri Carlo G., Haverty Carrie, Evans Eric A., Prenatal Diagnosis . 2017,第5期

机译：低胎儿馏分的非侵入性产前筛选：比较全基因组测序和单核苷酸多态性方法
2. Response to “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods” [J] . Muzzey Dale, Haverty Carrie, Evans Eric A., Prenatal Diagnosis . 2017,第7期

机译：对“低胎儿馏分的非侵入性产前筛选的反应：全基因组测序和单核苷酸多态性方法的比较”
3. Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods” [J] . Ryan Allison, Martin Kimberly A. Prenatal Diagnosis . 2017,第7期

机译：评论“低胎儿分数下的非侵袭产前筛选：比较全基因组测序和单核苷酸多态性方法”
4. FAST SCREENING OF SINGLE-NUCLEOTIDE POLYMORPHISMS USING CHIP-BASED TEMPERATURE GRADIENT CAPILLARY ELECTROPHORESIS [C] . Peng Liu, Wan-Li Xing, Dong Liang, International conference on miniaturized chemical and biochemical analysis systems . 2002

机译：基于芯片的温度梯度毛细管电泳快速筛选单核苷酸多态性
5. Development and application of a fetal epigenetic marker for noninvasive prenatal diagnosis [D] . Tong, Yu Kwan 2007

机译：胎儿表观遗传标记物在无创产前诊断中的开发与应用
6. Comment on Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods [O] . Allison Ryan, Kimberly A. Martin -1

机译：关于低胎儿无创产前筛查：比较全基因组测序和单核苷酸多态性方法的评论
7. Response to “Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods” [O] . Dale Muzzey, Carrie Haverty, Eric A. Evans, 2017

机译：对“低胎儿分数的非侵入产前筛选的反应：比较全基因组测序和单核苷酸多态性方法”

Noninvasive Prenatal Screening at Low Fetal Fraction: Comparing Whole-Genome Sequencing and Single-Nucleotide Polymorphism Methods

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