-
1
-
-
0342618532
-
Presence of fetal DNA in maternal plasma and serum
-
Lo YM, Corbetta N, Chamberlain PF, et al. Presence of fetal DNA in maternal plasma and serum. Lancet 1997;350(9076):485-7
-
(1997)
Lancet
, vol.350
, Issue.9076
, pp. 485-487
-
-
Lo, Y.M.1
Corbetta, N.2
Chamberlain, P.F.3
-
2
-
-
84870549609
-
Chromosomal microarray versus karyotyping for prenatal diagnosis
-
Wapner RJ, Martin CL, Levy B, et al. Chromosomal microarray versus karyotyping for prenatal diagnosis. N Engl J Med 2012;367(23):2175-84
-
(2012)
N Engl J Med
, vol.367
, Issue.23
, pp. 2175-2184
-
-
Wapner, R.J.1
Martin, C.L.2
Levy, B.3
-
3
-
-
84926313341
-
Whole genome array as a first-line cytogenetic test in prenatal diagnosis
-
Srebniak MI, Van Opstal D, Joosten M, et al. Whole genome array as a first-line cytogenetic test in prenatal diagnosis. Ultrasound Obstet Gynecol 2014;45(4):363-72
-
(2014)
Ultrasound Obstet Gynecol
, vol.45
, Issue.4
, pp. 363-372
-
-
Srebniak, M.I.1
Van Opstal, D.2
Joosten, M.3
-
4
-
-
84864879854
-
Diagnostic interpretation of array data using public databases and internet sources
-
de Leeuw N, Dijkhuizen T, Hehir-Kwa JY, et al. Diagnostic interpretation of array data using public databases and internet sources. Hum Mutat 2012;33(6):930-40
-
(2012)
Hum Mutat
, vol.33
, Issue.6
, pp. 930-940
-
-
De Leeuw, N.1
Dijkhuizen, T.2
Hehir-Kwa, J.Y.3
-
5
-
-
79960812993
-
Working Group of the American College of Medical Genetics Laboratory Quality Assurance C: American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants
-
Kearney HM, Thorland EC, Brown KK, et al. Working Group of the American College of Medical Genetics Laboratory Quality Assurance C: American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants. Genet Med 2011;13:680-5
-
(2011)
Genet Med
, vol.13
, pp. 680-685
-
-
Kearney, H.M.1
Thorland, E.C.2
Brown, K.K.3
-
6
-
-
84902353139
-
Types of array findings detectable in cytogenetic diagnosis: A proposal for a generic classification
-
Srebniak MI, Diderich KE, Govaerts LC, et al. Types of array findings detectable in cytogenetic diagnosis: a proposal for a generic classification. Eur J Hum Genet 2014;22(7):856-8
-
(2014)
Eur J Hum Genet
, vol.22
, Issue.7
, pp. 856-858
-
-
Srebniak, M.I.1
Diderich, K.E.2
Govaerts, L.C.3
-
7
-
-
84896691791
-
DNA sequencing versus standard prenatal aneuploidy screening
-
Bianchi DW, Parker RL, Wentworth J, et al. DNA sequencing versus standard prenatal aneuploidy screening. N Engl J Med 2014;370(9):799-808
-
(2014)
N Engl J Med
, vol.370
, Issue.9
, pp. 799-808
-
-
Bianchi, D.W.1
Parker, R.L.2
Wentworth, J.3
-
8
-
-
84908296065
-
Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing
-
Dar P, Curnow KJ, Gross SJ, et al. Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing. Am J Obstet Gynecol 2014;211(5):527.e1-527.e17
-
(2014)
Am J Obstet Gynecol
, vol.211
, Issue.5
, pp. 527e1-527e17
-
-
Dar, P.1
Curnow, K.J.2
Gross, S.J.3
-
9
-
-
84928601078
-
Noninvasive prenatal testing for trisomy 21, 18 and 13 - Clinical experience from 146,958 pregnancies
-
Zhang H, Gao Y, Jiang F, et al. Noninvasive prenatal testing for trisomy 21, 18 and 13 - clinical experience from 146,958 pregnancies. Ultrasound Obstet Gynecol 2015;45(5):530-8
-
(2015)
Ultrasound Obstet Gynecol
, vol.45
, Issue.5
, pp. 530-538
-
-
Zhang, H.1
Gao, Y.2
Jiang, F.3
-
10
-
-
84926492837
-
Cell-free DNA analysis for noninvasive examination of trisomy
-
Norton ME, Jacobsson B, Swamy GK, et al. Cell-free DNA analysis for noninvasive examination of trisomy. N Engl J Med 2015;372:1589-97
-
(2015)
N Engl J Med
, vol.372
, pp. 1589-1597
-
-
Norton, M.E.1
Jacobsson, B.2
Swamy, G.K.3
-
11
-
-
84920800389
-
Performance of non-invasive prenatal testing when fetal cell-free DNA is absent
-
Takoudes T and Hamar B. Performance of non-invasive prenatal testing when fetal cell-free DNA is absent. Ultrasound Obstet Gynecol 2015;45(1):112
-
(2015)
Ultrasound Obstet Gynecol
, vol.45
, Issue.1
, pp. 112
-
-
Takoudes, T.1
Hamar, B.2
-
12
-
-
84924766673
-
Expanding the scope of noninvasive prenatal testing: Detection of fetal microdeletion syndromes
-
Wapner RJ, Babiarz JE, Levy B, et al. Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes. Am J Obstet Gynecol 2014;212(3):332.e1-9
-
(2014)
Am J Obstet Gynecol
, vol.212
, Issue.3
, pp. 332e1-3329
-
-
Wapner, R.J.1
Babiarz, J.E.2
Levy, B.3
-
13
-
-
84920848763
-
Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: A systematic review and meta-analysis
-
Akolekar R, Beta J, Picciarelli G, et al. Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis. Ultrasound Obstet Gynecol 2015;45(1):16-26
-
(2015)
Ultrasound Obstet Gynecol
, vol.45
, Issue.1
, pp. 16-26
-
-
Akolekar, R.1
Beta, J.2
Picciarelli, G.3
-
14
-
-
84887080693
-
Noninvasive prenatal methylomic analysis by genomewide bisulfite sequencing of maternal plasma DNA
-
Lun FM, Chiu RW, Sun K, et al. Noninvasive prenatal methylomic analysis by genomewide bisulfite sequencing of maternal plasma DNA. Clin Chem 2013;59(11):1583-94
-
(2013)
Clin Chem
, vol.59
, Issue.11
, pp. 1583-1594
-
-
Lun, F.M.1
Chiu, R.W.2
Sun, K.3
-
15
-
-
84903731165
-
Maternal plasma RNA sequencing for genome-wide transcriptomic profiling and identification of pregnancy-associated transcripts
-
Tsui NB, Jiang P, Wong YF, et al. Maternal plasma RNA sequencing for genome-wide transcriptomic profiling and identification of pregnancy-associated transcripts. Clin Chem 2014;60(7):954-62
-
(2014)
Clin Chem
, vol.60
, Issue.7
, pp. 954-962
-
-
Tsui, N.B.1
Jiang, P.2
Wong, Y.F.3
-
16
-
-
84894316199
-
Review: Cell-free fetal DNA in the maternal circulation as an indicator of placental health and disease
-
Taglauer ES, Wilkins-Haug L and Bianchi DW. Review: Cell-free fetal DNA in the maternal circulation as an indicator of placental health and disease. Placenta 2014;35:S64-8
-
(2014)
Placenta
, vol.35
, pp. S64-S68
-
-
Taglauer, E.S.1
Wilkins-Haug, L.2
Bianchi, D.W.3
-
17
-
-
84889080221
-
Non-invasive prenatal testing using massively parallel sequencing of maternal plasma DNA: From molecular karyotyping to fetal whole-genome sequencing
-
Lo YMD. Non-invasive prenatal testing using massively parallel sequencing of maternal plasma DNA: from molecular karyotyping to fetal whole-genome sequencing. Reprod Biomed Online 2013;27(6):593-8
-
(2013)
Reprod Biomed Online
, vol.27
, Issue.6
, pp. 593-598
-
-
Ymd, L.1
|