-
1
-
-
0034936891
-
Maternal anxiety induced by prenatal diagnostic techniques: detection and management
-
Hertling-Schaal E, Perrotin F, de Poncheville L, et al. Maternal anxiety induced by prenatal diagnostic techniques: detection and management. Gynecol Obstet Fertil 2001;29(6):440-6.
-
(2001)
Gynecol Obstet Fertil
, vol.29
, Issue.6
, pp. 440-446
-
-
Hertling-Schaal, E.1
Perrotin, F.2
de Poncheville, L.3
-
2
-
-
33846644997
-
Amniocentesis results: investigation of anxiety. The ARIA trial
-
iii, ix-x
-
Hewison J, Nixon J, Fountain J, et al. Amniocentesis results: investigation of anxiety. The ARIA trial. Health Technol Assess 2006;10(50):iii, ix-x, 1-78.
-
(2006)
Health Technol Assess
, vol.10
, Issue.50
, pp. 1-78
-
-
Hewison, J.1
Nixon, J.2
Fountain, J.3
-
3
-
-
33847789507
-
A randomised trial of two methods of issuing prenatal test results: the ARIA (Amniocentesis Results: Investigation of Anxiety) trial
-
Hewison J, Nixon J, Fountain J, et al. A randomised trial of two methods of issuing prenatal test results: the ARIA (Amniocentesis Results: Investigation of Anxiety) trial. BJOG 2007;114(4):462-8.
-
(2007)
BJOG
, vol.114
, Issue.4
, pp. 462-468
-
-
Hewison, J.1
Nixon, J.2
Fountain, J.3
-
4
-
-
34548405957
-
Procedure-related complications of amniocentesis and chorionic villous sampling: a systematic review
-
Mujezinovic F, Alfirevic Z. Procedure-related complications of amniocentesis and chorionic villous sampling: a systematic review. Obstet Gynecol 2007;110(3):687-94.
-
(2007)
Obstet Gynecol
, vol.110
, Issue.3
, pp. 687-694
-
-
Mujezinovic, F.1
Alfirevic, Z.2
-
5
-
-
42449152414
-
Revisiting the fetal loss rate after second-trimester genetic amniocentesis: a single center's 16-year experience
-
Odibo AO, Gray DL, Dicke JM, et al. Revisiting the fetal loss rate after second-trimester genetic amniocentesis: a single center's 16-year experience. Obstet Gynecol 2008;111(3):589-95.
-
(2008)
Obstet Gynecol
, vol.111
, Issue.3
, pp. 589-595
-
-
Odibo, A.O.1
Gray, D.L.2
Dicke, J.M.3
-
6
-
-
76449093190
-
Update on procedure-related risks for prenatal diagnosis techniques
-
Tabor A, Alfirevic Z. Update on procedure-related risks for prenatal diagnosis techniques. Fetal Diagn Ther 2010;27(1):1-7.
-
(2010)
Fetal Diagn Ther
, vol.27
, Issue.1
, pp. 1-7
-
-
Tabor, A.1
Alfirevic, Z.2
-
7
-
-
0022650629
-
Randomised controlled trial of genetic amniocentesis in 4606 low-risk women
-
Tabor A, Philip J, Madsen M, et al. Randomised controlled trial of genetic amniocentesis in 4606 low-risk women. Lancet 1986;1(8493):1287-93.
-
(1986)
Lancet
, vol.1
, Issue.8493
, pp. 1287-1293
-
-
Tabor, A.1
Philip, J.2
Madsen, M.3
-
8
-
-
84860213983
-
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing
-
Bianchi DW, Platt LD, Goldberg JD, et al. Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing. Obstet Gynecol 2012;119(5):890-901.
-
(2012)
Obstet Gynecol
, vol.119
, Issue.5
, pp. 890-901
-
-
Bianchi, D.W.1
Platt, L.D.2
Goldberg, J.D.3
-
9
-
-
79952302397
-
Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting
-
205 e1-205 11
-
Ehrich M, Deciu C, Zwiefelhofer T, et al. Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting. Am J Obstet Gynecol 2011;204(3):205 e1-11.
-
(2011)
Am J Obstet Gynecol
, vol.204
, Issue.3
-
-
Ehrich, M.1
Deciu, C.2
Zwiefelhofer, T.3
-
10
-
-
84857868297
-
DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study
-
Palomaki GE, Deciu C, Kloza EM, et al. DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study. Genet Med 2012;14(3):296-305.
-
(2012)
Genet Med
, vol.14
, Issue.3
, pp. 296-305
-
-
Palomaki, G.E.1
Deciu, C.2
Kloza, E.M.3
-
11
-
-
80755172331
-
DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study
-
Palomaki GE, Kloza EM, Lambert-Messerlian GM, et al. DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study. Genet Med 2011;13(11):913-20.
-
(2011)
Genet Med
, vol.13
, Issue.11
, pp. 913-920
-
-
Palomaki, G.E.1
Kloza, E.M.2
Lambert-Messerlian, G.M.3
-
12
-
-
84863574483
-
Detection of microdeletion 22q11.2 in a fetus by next-generation sequencing of maternal plasma
-
Jensen TJ, Dzakula Z, Deciu C, et al. Detection of microdeletion 22q11.2 in a fetus by next-generation sequencing of maternal plasma. Clin Chem 2012;58(7):1148-51.
-
(2012)
Clin Chem
, vol.58
, Issue.7
, pp. 1148-1151
-
-
Jensen, T.J.1
Dzakula, Z.2
Deciu, C.3
-
13
-
-
80955166920
-
Noninvasive prenatal diagnosis of a fetal microdeletion syndrome
-
Peters D, Chu T, Yatsenko SA, et al. Noninvasive prenatal diagnosis of a fetal microdeletion syndrome. N Engl J Med 2011;365(19):1847-8.
-
(2011)
N Engl J Med
, vol.365
, Issue.19
, pp. 1847-1848
-
-
Peters, D.1
Chu, T.2
Yatsenko, S.A.3
-
14
-
-
84873711791
-
Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma
-
Srinivasan A, Bianchi DW, Huang H, et al. Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma. Am J Hum Genet 2013;92(2):167-76.
-
(2013)
Am J Hum Genet
, vol.92
, Issue.2
, pp. 167-176
-
-
Srinivasan, A.1
Bianchi, D.W.2
Huang, H.3
-
15
-
-
84876269433
-
Noninvasive prenatal molecular karyotyping from maternal plasma
-
Yu SC, Jiang P, Choy KW, et al. Noninvasive prenatal molecular karyotyping from maternal plasma. PLoS One 2013;8(4):e60968.
-
(2013)
PLoS One
, vol.8
, Issue.4
-
-
Yu, S.C.1
Jiang, P.2
Choy, K.W.3
-
16
-
-
78650632807
-
Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis
-
Hillman SC, Pretlove S, Coomarasamy A, et al. Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis. Ultrasound Obstet Gynecol 2011;37(1):6-14.
-
(2011)
Ultrasound Obstet Gynecol
, vol.37
, Issue.1
, pp. 6-14
-
-
Hillman, S.C.1
Pretlove, S.2
Coomarasamy, A.3
-
17
-
-
84866999347
-
Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies
-
Shaffer LG, Dabell MP, Fisher AJ, et al. Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies. Prenat Diagn 2012;32(10):976-85.
-
(2012)
Prenat Diagn
, vol.32
, Issue.10
, pp. 976-985
-
-
Shaffer, L.G.1
Dabell, M.P.2
Fisher, A.J.3
-
18
-
-
77649235558
-
Deletion and point mutations of PTHLH cause brachydactyly type E
-
Klopocki E, Hennig BP, Dathe K, et al. Deletion and point mutations of PTHLH cause brachydactyly type E. Am J Hum Genet 2010;86(3):434-9.
-
(2010)
Am J Hum Genet
, vol.86
, Issue.3
, pp. 434-439
-
-
Klopocki, E.1
Hennig, B.P.2
Dathe, K.3
-
19
-
-
55849124028
-
Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood
-
Fan HC, Blumenfeld YJ, Chitkara U, et al. Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood. Proc Natl Acad Sci U S A 2008;105(42):16266-71.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, Issue.42
, pp. 16266-16271
-
-
Fan, H.C.1
Blumenfeld, Y.J.2
Chitkara, U.3
-
20
-
-
0347898005
-
Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis
-
Lo YM, Tein MS, Lau TK, et al. Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. Am J Hum Genet 1998;62(4):768-75.
-
(1998)
Am J Hum Genet
, vol.62
, Issue.4
, pp. 768-775
-
-
Lo, Y.M.1
Tein, M.S.2
Lau, T.K.3
-
21
-
-
67649958254
-
Non-invasive prenatal diagnosis by single molecule counting technologies
-
Chiu RW, Cantor CR, Lo YM. Non-invasive prenatal diagnosis by single molecule counting technologies. Trends Genet 2009;25(7):324-31.
-
(2009)
Trends Genet
, vol.25
, Issue.7
, pp. 324-331
-
-
Chiu, R.W.1
Cantor, C.R.2
Lo, Y.M.3
-
22
-
-
65549102180
-
Statistical model for whole genome sequencing and its application to minimally invasive diagnosis of fetal genetic disease
-
Chu T, Bunce K, Hogge WA, et al. Statistical model for whole genome sequencing and its application to minimally invasive diagnosis of fetal genetic disease. Bioinformatics 2009;25(10):1244-50.
-
(2009)
Bioinformatics
, vol.25
, Issue.10
, pp. 1244-1250
-
-
Chu, T.1
Bunce, K.2
Hogge, W.A.3
-
23
-
-
0002294347
-
A simple sequentially rejective multiple test procedure
-
Holm S. A simple sequentially rejective multiple test procedure. Scand J Stat 1979;6:65-70.
-
(1979)
Scand J Stat
, vol.6
, pp. 65-70
-
-
Holm, S.1
-
24
-
-
0023710206
-
Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach
-
DeLong ER, DeLong DM, Clarke-Pearson DL. Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach. Biometrics 1988;44(3):837-45.
-
(1988)
Biometrics
, vol.44
, Issue.3
, pp. 837-845
-
-
DeLong, E.R.1
DeLong, D.M.2
Clarke-Pearson, D.L.3
-
25
-
-
58149490683
-
Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma
-
Chiu RW, Chan KC, Gao Y, et al. Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma. Proc Natl Acad Sci U S A 2008;105(51):20458-63.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, Issue.51
, pp. 20458-20463
-
-
Chiu, R.W.1
Chan, K.C.2
Gao, Y.3
-
26
-
-
34547664096
-
Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes
-
Lupski JR, Stankiewicz P. Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes. PLoS Genet 2005;1(6):e49.
-
(2005)
PLoS Genet
, vol.1
, Issue.6
-
-
Lupski, J.R.1
Stankiewicz, P.2
-
27
-
-
0034513406
-
Molecular mechanisms for constitutional chromosomal rearrangements in humans
-
Shaffer LG, Lupski JR. Molecular mechanisms for constitutional chromosomal rearrangements in humans. Annu Rev Genet 2000;34:297-329.
-
(2000)
Annu Rev Genet
, vol.34
, pp. 297-329
-
-
Shaffer, L.G.1
Lupski, J.R.2
|