低深度全基因组测序技术在产前诊断中的应用专家共识
[1] 染色体微阵列分析技术在产前诊断中的应用协作组.染色体微阵列分析技术在产前诊断中的应用专家共识[J].中华妇产科杂志.2014,(8).DOI:10.3760/cma.j.issn.0529-567x.2014.08.002 .
[2] Jing, Wang,Lin, Chen,Cong, Zhou,等.Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.[J].American Journal of Obstetrics & Gynecology.2018,(Spec ).DOI:10.1016/j.ajog.2018.05.030 .
[3] Zhu, Xiangyu,Li, Jie,Ru, Tong,等.Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing[J].Prenatal Diagnosis.2016,36(4).321-327.DOI:10.1002/pd.4782 .
[4] Evans, Mark I.,Wapner, Ronald J.,Berkowitz, Richard L..Noninvasive prenatal screening or advanced diagnostic testing: caveat emptor[J].American Journal of Obstetrics and Gynecology.2016,215(3).298-305.DOI:10.1016/j.ajog.2016.04.029 .
[5] Cohen, K.,Tzika, A.,Wood, H.,等.Diagnosis of fetal submicroscopic chromosomal abnormalities in failed array CGH samples: copy number by sequencing as an alternative to microarrays for invasive fetal testing[J].Ultrasound in obstetrics & gynecology: the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.2015,45(4).394-401.DOI:10.1002/uog.14767 .
[6] S, Liu,L, Song,D S, Cram,等.Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage.[J].Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.2015,46(4).472-7.DOI:10.1002/uog.14849 .
[7] Wang,Y.,Chen,Y.,Tian,F.,等.Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing[J].Clinical Chemistry: Journal of the American Association for Clinical Chemists.2014,60(1).251-259.DOI:10.1373/clinchem.2013.215145 .
[8] Julián, Nevado,Rafaella, Mergener,María, Palomares-Bralo,等.New microdeletion and microduplication syndromes: A comprehensive review.[J].Genetics & Molecular Biology.2014.37210-9.
[9] Jun Mao,Ting Wang,Ben-Jing Wang,等.Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy[J].Clinica chimica acta: International journal of clinical chemistry & applied molecular biology.2014.433
[10] Wang,Y.,Zhu,J.,Chen,Y.,等.Two cases of placental T21 mosaicism: Challenging the detection limits of non-invasive prenatal testing[J].Prenatal Diagnosis.2013,33(12).
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