-
1
-
-
84870156368
-
-
Noninvasive prenatal testing for fetal aneuploidy. Committee Opinion No. 545. American College of Obstetricians and Gynecologists. Obstet Gynecol 2012;120:1532-4.
-
(2012)
Obstet Gynecol
, vol.120
, pp. 1532-1534
-
-
-
2
-
-
84880045096
-
Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis
-
Benn P, Borell A, Chiu R Cuckle H, Dugoff L, Faas B, et al. Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis. Prenat Diagn 2013;33:622-9.
-
(2013)
Prenat Diagn
, vol.33
, pp. 622-629
-
-
Benn, P.1
Borell, A.2
Chiu Cuckle R, H.3
Dugoff, L.4
Faas, B.5
-
3
-
-
84879494122
-
Current status in non-invasive prenatal detection of Down syndrome, trisomy 18, and trisomy 13 using cell-free DNA in maternal plasma
-
Langlois S, Brock JA; Genetics Committee, Wilson RD, Audibert F, Brock JA, et al. Current status in non-invasive prenatal detection of Down syndrome, trisomy 18, and trisomy 13 using cell-free DNA in maternal plasma. J Obstet Gynaecol Can 2013;35:177-83.
-
(2013)
J Obstet Gynaecol Can
, vol.35
, pp. 177-183
-
-
Langlois, S.1
Brock, J.A.2
Wilson, R.D.3
Audibert, F.4
Brock, J.A.5
-
4
-
-
84877253478
-
ACMG statement on noninvasive prenatal screening for fetal aneuploidy
-
Gregg AR Gross SJ, Best RG, Monaghan KG, Bajaj K, Skotko BG, et al. ACMG statement on noninvasive prenatal screening for fetal aneuploidy. Genet Med 2013;15:395-8.
-
(2013)
Genet Med
, vol.15
, pp. 395-398
-
-
Gregg, A.R.1
Gross, S.J.2
Best, R.G.3
Monaghan, K.G.4
Bajaj, K.5
Skotko, B.G.6
-
5
-
-
84877926367
-
Noninvasive prenatal testing/noninvasive prenatal diagnosis: The position of the National Society of Genetic Counselors
-
Devers PL, Cronister A, Ormond KE, Facio F, Brasington CK, Flodman P. Noninvasive prenatal testing/noninvasive prenatal diagnosis: the position of the National Society of Genetic Counselors.J Genet Couns 2013;22:291-5.
-
(2013)
J Genet Couns
, vol.22
, pp. 291-295
-
-
Devers, P.L.1
Cronister, A.2
Ormond, K.E.3
Facio, F.4
Brasington, C.K.5
Flodman, P.6
-
6
-
-
84874616358
-
High-throughput massively parallel sequencing for fetal aneuploidy detection from maternal plasma
-
Jensen TJ, Zwiefelhofer T, Tim RC, Dzakula Z, Kim SK, Mazloom AR et al. High-throughput massively parallel sequencing for fetal aneuploidy detection from maternal plasma. PLoS One 2013;8:e57381.
-
(2013)
PLoS One
, vol.8
, pp. e57381
-
-
Jensen, T.J.1
Zwiefelhofer, T.2
Tim, R.C.3
Dzakula, Z.4
Kim, S.K.5
Mazloom, A.R.6
-
7
-
-
80755172331
-
DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study
-
Palomaki GE, Kloza EM, Lambert-Messerlian GM, HaddowJE, Neveux LM, Ehrich M, et al. DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study. Genet Med 2011;13:913-20.
-
(2011)
Genet Med
, vol.13
, pp. 913-920
-
-
Palomaki, G.E.1
Kloza, E.M.2
Lambert-Messerlian, G.M.3
Haddow, J.E.4
Neveux, L.M.5
Ehrich, M.6
-
8
-
-
77955255742
-
Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics
-
Fan HC, Quake SR Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics. PLoS One 2010;5:e10439.
-
(2010)
PLoS One
, vol.5
, pp. e10439
-
-
Fan, H.C.1
Quake, S.R.2
-
9
-
-
84896500248
-
Maternal plasma fetal DNA fractions in pregnancies with low and high risks for fetal chromosomal aneuploidies
-
Hudecova I, Sahota D, Heung MM, Jin Y, Lee WS, Leung TY, et al. Maternal plasma fetal DNA fractions in pregnancies with low and high risks for fetal chromosomal aneuploidies. PLoS One 2014;9:e88484.
-
(2014)
PLoS One
, vol.9
, pp. e88484
-
-
Hudecova, I.1
Sahota, D.2
Heung, M.M.3
Jin, Y.4
Lee, W.S.5
Leung, T.Y.6
-
10
-
-
84907705050
-
Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA
-
Porreco RP, Garite TJ, Maurel K Marusiak B; Obstetrix Collaborative Research Network, Ehrich M, et al. Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA. Am J Obstet Gynecol 2014;211:365.e1-12.
-
(2014)
Am J Obstet Gynecol
, vol.211
, pp. 365e1-36512
-
-
Porreco, R.P.1
Garite, T.J.2
Maurel, K.3
Marusiak, B.4
Ehrich, M.5
-
11
-
-
78751683468
-
Non-invasive prenatal assessment of trisomy 21 by multiplex maternal plasma DNA sequencing: Large scale validity study
-
Chiu RW, Akolekar R, Zheng YW, Leung TY, Sun H, Chan KC, et al. Non-invasive prenatal assessment of trisomy 21 by multiplex maternal plasma DNA sequencing: large scale validity study. BMJ 2011;342:c7401.
-
(2011)
BMJ
, vol.342
, pp. c7401
-
-
Chiu, R.W.1
Akolekar, R.2
Zheng, Y.W.3
Leung, T.Y.4
Sun, H.5
Chan, K.C.6
-
12
-
-
79952302397
-
Non invasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: A study in a clinical setting
-
Ehrich M, Deciu C, Zwiefelhofer T, Tynan JA, Cagasan L, Tim R, et al. Non invasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting. Am J Obstet Gynecol 2011;204:205.e1-11.
-
(2011)
Am J Obstet Gynecol
, vol.204
, pp. 205e1-20511
-
-
Ehrich, M.1
Deciu, C.2
Zwiefelhofer, T.3
Tynan, J.A.4
Cagasan, L.5
Tim, R.6
-
13
-
-
84860213983
-
Genome wide fetal aneuploidy detection by maternal plasma DNA sequencing
-
Bianchi DW, Platt LD, Goldberg JD, Abuhamad AZ, Sehnert AJ, Rava RP; MatErnal BLood IS Source to Accurately diagnose fetal aneuploidy (MELISSA) Study Group. Genome wide fetal aneuploidy detection by maternal plasma DNA sequencing. Obstet Gynecol 2012;119:890-901.
-
(2012)
Obstet Gynecol
, vol.119
, pp. 890-901
-
-
Bianchi, D.W.1
Platt, L.D.2
Goldberg, J.D.3
Abuhamad, A.Z.4
Sehnert, A.J.5
Rava, R.P.6
-
14
-
-
84870688045
-
Clinical application of massively parallel sequencing based prenatal non invasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors
-
Dan S, Wang W, Ren J, Li Y, Hu H, Xu Z, et al. Clinical application of massively parallel sequencing based prenatal non invasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors. Prenat Diagn 2012;32:1225-32.
-
(2012)
Prenat Diagn
, vol.32
, pp. 1225-1232
-
-
Dan, S.1
Wang, W.2
Ren, J.3
Li, Y.4
Hu, H.5
Xu, Z.6
-
15
-
-
84859361254
-
Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: Evaluation for trisomy 21 and trisomy 18
-
Sparks AB, Struble CA, Wang ET, Song K, Oliphant A. Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18. Am J Obstet Gynecol 2012; 206:319.e1-9.
-
(2012)
Am J Obstet Gynecol
, vol.206
, pp. 319e1-3199
-
-
Sparks, A.B.1
Struble, C.A.2
Wang, E.T.3
Song, K.4
Oliphant, A.5
-
16
-
-
84908296065
-
Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneu-ploidy testing
-
Dar P, Curnow KJ, Gross SJ, Hall MP, Stosic M, Demko Z, et al. Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneu-ploidy testing. Am J Obstet Gynecol 2014;211:527.e1-17.
-
(2014)
Am J Obstet Gynecol
, vol.211
, pp. 527e1-52717
-
-
Dar, P.1
Curnow, K.J.2
Gross, S.J.3
Hall, M.P.4
Stosic, M.5
Demko, Z.6
-
17
-
-
84905093469
-
Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort
-
Pergament E, Cuckle H, Zimmermann B, Banjevic M, Sigurjonsson S, Ryan A, et al. Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort. Obstet Gynecol 2014;124:210-8.
-
(2014)
Obstet Gynecol
, vol.124
, pp. 210-218
-
-
Pergament, E.1
Cuckle, H.2
Zimmermann, B.3
Banjevic, M.4
Sigurjonsson, S.5
Ryan, A.6
-
18
-
-
84924256744
-
Circulating cell free DNA testing: Are some test failures informative?
-
Palomaki G, Kloza E, Lambert-Messerlian G, van den Boom D, Ehrich M, Deciu C, et al. Circulating cell free DNA testing: are some test failures informative? Prenat Diagn 2015;35:289-93.
-
(2015)
Prenat Diagn
, vol.35
, pp. 289-293
-
-
Palomaki, G.1
Kloza, E.2
Lambert-Messerlian, G.3
Van Den Boom, D.4
Ehrich, M.5
Deciu, C.6
-
19
-
-
84907717938
-
Non-invasive prenatal chromosomal aneu-ploidy testing-clinical experience: 100,000 clinical samples
-
McCullough RM, Almasri EA, Guan X, Geis JA, Hicks SC, Mazloom AR, et al. Non-invasive prenatal chromosomal aneu-ploidy testing-clinical experience: 100,000 clinical samples. PLoS One 2014;9:e109173.
-
(2014)
PLoS One
, vol.9
, pp. e109173
-
-
McCullough, R.M.1
Almasri, E.A.2
Guan, X.3
Geis, J.A.4
Hicks, S.C.5
Mazloom, A.R.6
-
20
-
-
84922462757
-
Maternal source of false-positive fetal sex chromosome aneuploidy in noninvasive prenatal testing
-
McNamara CJ, Limone LA, Westover T, Miller RC. Maternal source of false-positive fetal sex chromosome aneuploidy in noninvasive prenatal testing. Obstet Gynecol 2015;125:390-2.
-
(2015)
Obstet Gynecol
, vol.125
, pp. 390-392
-
-
McNamara, C.J.1
Limone, L.A.2
Westover, T.3
Miller, R.C.4
-
21
-
-
84929849385
-
Noninvasive prenatal testing compared with invasive diagnostic testing in the setting of an abnormal state aneu-ploidy screen
-
Rad S, Turner AL, Beauchamp S, Aghajanian P, Williams J III, Esakoff TF. Noninvasive prenatal testing compared with invasive diagnostic testing in the setting of an abnormal state aneu-ploidy screen. Obstet Gynecol 2014;123(suppl 1):100S.
-
(2014)
Obstet Gynecol
, vol.123
, pp. 100S
-
-
Rad, S.1
Turner, A.L.2
Beauchamp, S.3
Aghajanian, P.4
Williams Iii., J.5
Esakoff, T.F.6
-
22
-
-
84920861342
-
Chromosomal microarray in fetuses with increased nuchal trans-lucency
-
Lund IC, Christensen R, Petersen OB, Vogel I, Vestergaard EM. Chromosomal microarray in fetuses with increased nuchal trans-lucency. Ultrasound Obstet Gynecol 2015;45:95-100.
-
(2015)
Ultrasound Obstet Gynecol
, vol.45
, pp. 95-100
-
-
Lund, I.C.1
Christensen, R.2
Petersen, O.B.3
Vogel, I.4
Vestergaard, E.M.5
-
23
-
-
84893182999
-
The use of chromosomal microarray analysis in prenatal diagnosis
-
The use of chromosomal microarray analysis in prenatal diagnosis. Committee Opinion No. 581. American College of Obstetricians and Gynecologists. Obstet Gynecol 2013; 122:1374-7.
-
(2013)
Obstet Gynecol
, vol.122
, pp. 1374-1377
-
-
|