-
3
-
-
0017316806
-
Midtrimester amniocentesis for prenatal diagnosis. Safety and accuracy
-
10.1001/jama.236.13.1471 989112
-
Midtrimester amniocentesis for prenatal diagnosis. Safety and accuracy JAMA 1976, 236:1471-1476. 10.1001/jama.236.13.1471 989112
-
(1976)
JAMA
, vol.236
, pp. 1471-1476
-
-
-
4
-
-
0035708466
-
The diagnostic performance of cytogenetic investigation in amniotic fluid cells and chorionic villi2
-
10.1002/pd.194 11787042
-
Los FJ Van den BC Wildschut HI Brandenburg H den Hollander NS Schoonderwaldt EM Pijpers L Jan HG Van Opstal D The diagnostic performance of cytogenetic investigation in amniotic fluid cells and chorionic villi2 Prenat Diagn 2001, 21:1150-1158. 10.1002/pd.194 11787042
-
(2001)
Prenat Diagn
, vol.21
, pp. 1150-1158
-
-
Los, F.J.1
Van den, B.C.2
Wildschut, H.I.3
Brandenburg, H.4
den Hollander, N.S.5
Schoonderwaldt, E.M.6
Pijpers, L.7
Jan, H.G.8
Van Opstal, D.9
-
5
-
-
0038207040
-
Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities4
-
12773259
-
Grimshaw GM Szczepura A Hulten M MacDonald F Nevin NC Sutton F Dhanjal S Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities4 Health Technol Assess 2003, 7:1-146. 12773259
-
(2003)
Health Technol Assess
, vol.7
, pp. 1-146
-
-
Grimshaw, G.M.1
Szczepura, A.2
Hulten, M.3
MacDonald, F.4
Nevin, N.C.5
Sutton, F.6
Dhanjal, S.7
-
7
-
-
33845235003
-
High-throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy2
-
10.1002/ajmg.a.31552
-
Bruno DL Burgess T Ren H Nouri S Pertile MD Francis DI Norris F Kenney BK Schouten J Choo KHA Slater HR High-throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy2 American Journal of Medical Genetics Part A 2006, 140A:2786-2793. 10.1002/ajmg.a.31552
-
(2006)
American Journal of Medical Genetics Part A
, vol.140 A
, pp. 2786-2793
-
-
Bruno, D.L.1
Burgess, T.2
Ren, H.3
Nouri, S.4
Pertile, M.D.5
Francis, D.I.6
Norris, F.7
Kenney, B.K.8
Schouten, J.9
Choo, K.H.A.10
Slater, H.R.11
-
8
-
-
13544268702
-
Computer-assisted prenatal aneuploidy screening for chromosome 13, 18, 21, X and Y based on multiplex ligation-dependent probe amplification (MLPA)
-
10.1038/sj.ejhg.5201307 15483643
-
Gerdes T Kirchhoff M Lind AM Larsen GV Schwartz M Lundsteen C Computer-assisted prenatal aneuploidy screening for chromosome 13, 18, 21, X and Y based on multiplex ligation-dependent probe amplification (MLPA) Eur J Hum Genet 2005, 13:171-175. 10.1038/sj.ejhg.5201307 15483643
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 171-175
-
-
Gerdes, T.1
Kirchhoff, M.2
Lind, A.M.3
Larsen, G.V.4
Schwartz, M.5
Lundsteen, C.6
-
9
-
-
1642544630
-
Rapid, high throughput prenatal detection of aneuploidy using a novel quantitative method (MLPA)
-
1735348 14684689 10.1136/jmg.40.12.907
-
Slater HR Bruno DL Ren H Pertile M Schouten JP Choo KH Rapid, high throughput prenatal detection of aneuploidy using a novel quantitative method (MLPA) J Med Genet 2003, 40:907-912. 1735348 14684689 10.1136/ jmg.40.12.907
-
(2003)
J Med Genet
, vol.40
, pp. 907-912
-
-
Slater, H.R.1
Bruno, D.L.2
Ren, H.3
Pertile, M.4
Schouten, J.P.5
Choo, K.H.6
-
10
-
-
28544432673
-
Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA)
-
10.1002/pd.1247 16231311
-
Hochstenbach R Meijer J van de BJ Vossebeld-Hoff I Jansen R van der Luijt RB Sinke RJ Page-Christiaens GC Ploos van Amstel JK de Pater JM Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA) Prenat Diagn 2005, 25:1032-1039. 10.1002/pd.1247 16231311
-
(2005)
Prenat Diagn
, vol.25
, pp. 1032-1039
-
-
Hochstenbach, R.1
Meijer, J.2
van de, B.J.3
Vossebeld-Hoff, I.4
Jansen, R.5
van der Luijt, R.B.6
Sinke, R.J.7
Page-Christiaens, G.C.8
Ploos van Amstel, J.K.9
de Pater, J.M.10
-
11
-
-
22244465516
-
Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: A cytogenetic risk assessment
-
10.1016/S0140-6736(05)66790-6 16005334
-
Caine A Maltby AE Parkin CA Waters JJ Crolla JA Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: A cytogenetic risk assessment Lancet 2005, 366:123-128. 10.1016/S0140-6736(05)66790-6 16005334
-
(2005)
Lancet
, vol.366
, pp. 123-128
-
-
Caine, A.1
Maltby, A.E.2
Parkin, C.A.3
Waters, J.J.4
Crolla, J.A.5
-
12
-
-
33644777447
-
Fetal nuchal translucency scan and early prenatal diagnosis of chromosomal abnormalities by rapid aneuploidy screening: Observational study11
-
1382537 16476673 10.1136/bmj.38730.655197.AE
-
Chitty LS Kagan KO Molina FS Waters JJ Nicolaides KH Fetal nuchal translucency scan and early prenatal diagnosis of chromosomal abnormalities by rapid aneuploidy screening: Observational study11 British Medical Journal 2006, 332:452-454. 1382537 16476673 10.1136/ bmj.38730.655197.AE
-
(2006)
British Medical Journal
, vol.332
, pp. 452-454
-
-
Chitty, L.S.1
Kagan, K.O.2
Molina, F.S.3
Waters, J.J.4
Nicolaides, K.H.5
-
13
-
-
0042021913
-
Rapid prenatal diagnosis of aneuploidies and zygosity in multiple pregnancies by amniocentesis with single insertion of the needle and quantitative fluorescent PCR
-
10.1002/pd.655 12913868
-
Cirigliano V Canadas P Plaja A Ordonez E Mediano C Sanchez A Farran I Rapid prenatal diagnosis of aneuploidies and zygosity in multiple pregnancies by amniocentesis with single insertion of the needle and quantitative fluorescent PCR Prenat Diagn 2003, 23:629-633. 10.1002/ pd.655 12913868
-
(2003)
Prenat Diagn
, vol.23
, pp. 629-633
-
-
Cirigliano, V.1
Canadas, P.2
Plaja, A.3
Ordonez, E.4
Mediano, C.5
Sanchez, A.6
Farran, I.7
-
14
-
-
22244493861
-
Rapid aneuploidy testing, traditional karyotyping, or both?
-
10.1016/S0140-6736(05)66791-8 16005312
-
Leung WC Lao TT Rapid aneuploidy testing, traditional karyotyping, or both? Lancet 2005, 366:97-98. 10.1016/S0140-6736(05)66791-8 16005312
-
(2005)
Lancet
, vol.366
, pp. 97-98
-
-
Leung, W.C.1
Lao, T.T.2
-
16
-
-
44649188217
-
-
M.A.K.E.study
-
M.A.K.E.study 2008 http://www.makestudy.nl/make/docs/about.asp
-
(2008)
-
-
-
17
-
-
33947237911
-
Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis
-
17290441 10.1002/ajmg.c.30114
-
Shaffer LG Bui TH Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis Am J Med Genet C Semin Med Genet 2007, 145C(1):87-98. 17290441 10.1002/ajmg.c.30114
-
(2007)
Am J Med Genet C Semin Med Genet
, vol.145 C
, Issue.1
, pp. 87-98
-
-
Shaffer, L.G.1
Bui, T.H.2
|