-
2
-
-
67149115401
-
Prenatal screening for aneuploidy
-
Driscoll DA, Gross S. Prenatal screening for aneuploidy. N Engl J Med 2009; 360: 2556-62.
-
(2009)
N Engl J Med
, vol.360
, pp. 2556-2562
-
-
Driscoll, D.A.1
Gross, S.2
-
3
-
-
34548405957
-
Procedure-related complications of amniocentesis and chorionic villous sampling: A systematic review
-
DOI 10.1097/01.AOG.0000278820.54029.e3, PII 0000625020070900000024
-
Mujezinovic F, Alfirevic Z. Procedure-related complications of amnio-centesis and chorionic villous sampling - A systematic review. Obstet Gynecol 2007; 110: 687-94. (Pubitemid 47359597)
-
(2007)
Obstetrics and Gynecology
, vol.110
, Issue.3
, pp. 687-694
-
-
Mujezinovic, F.1
Alfirevic, Z.2
-
4
-
-
0025364769
-
Isolation of fetal DNA from nucleated erythrocytes in maternal blood
-
DOI 10.1073/pnas.87.9.3279
-
Bianchi DW, Flint AF, Pizzimenti MF, et al. Isolation of fetal DNA from nucleated erythrocytes in maternal blood. Proc Natl Acad Sci USA 1990; 87: 3279-83. (Pubitemid 20173618)
-
(1990)
Proceedings of the National Academy of Sciences of the United States of America
, vol.87
, Issue.9
, pp. 3279-3283
-
-
Bianchi, D.W.1
Flint, A.F.2
Pizzimenti, M.F.3
Knoll, J.H.M.4
Latt, S.A.5
-
5
-
-
0030776456
-
PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies
-
Bianchi DW, Williams JM, Sullivan LM, et al. PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies. Am J Hum Genet 1997; 61: 822-9. (Pubitemid 27418456)
-
(1997)
American Journal of Human Genetics
, vol.61
, Issue.4
, pp. 822-829
-
-
Bianchi, D.W.1
Williams, J.M.2
Sullivan, L.M.3
Hanson, F.W.4
Klinger, K.W.5
Shuber, A.P.6
-
6
-
-
0030034519
-
Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum
-
DOI 10.1073/pnas.93.2.705
-
Bianchi DW, Zickwolf GK, Weil GJ, et al. Male fetal progenitor cells persist in maternal blood for as long as 27years postpartum. Proc Natl Acad Sci USA 1996; 93: 705-8. (Pubitemid 26041153)
-
(1996)
Proceedings of the National Academy of Sciences of the United States of America
, vol.93
, Issue.2
, pp. 705-708
-
-
Bianchi, D.W.1
Zickwolf, G.K.2
Weil, G.J.3
Sylvester, S.4
Demaria, M.A.5
-
7
-
-
0342618532
-
Presence of fetal DNA in maternal plasma and serum
-
DOI 10.1016/S0140-6736(97)02174-0
-
Lo YMD, Corbetta N, Chamberlain PF, et al. Presence of fetal DNA in maternal plasma and serum. Lancet 1997; 350: 485-7. (Pubitemid 27343304)
-
(1997)
Lancet
, vol.350
, Issue.9076
, pp. 485-487
-
-
Dennis Lo, Y.M.1
Corbetta, N.2
Chamberlain, P.F.3
Rai, V.4
Sargent, I.L.5
Redman, C.W.G.6
Wainscoat, J.S.7
-
8
-
-
34347230507
-
Free fetal DNA in maternal plasma in anembryonic pregnancies: Confirmation that the origin is the trophoblast
-
DOI 10.1002/pd.1700
-
Alberry M, Maddocks D, Jones M, et al. Free fetal DNA in maternal plasma in anembryonic pregnancies: confirmation that the origin is the trophoblast. Prenat Diagn 2007; 27: 415-8. (Pubitemid 47164339)
-
(2007)
Prenatal Diagnosis
, vol.27
, Issue.5
, pp. 415-418
-
-
Alberry, M.1
Maddocks, D.2
Jones, M.3
Abdel Hadi, M.4
Abdel-Fattah, S.5
Avent, N.6
Soothill, P.W.7
-
9
-
-
33845512998
-
Hypermethylated RASSF1A in maternal plasma: A universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis
-
DOI 10.1373/clinchem.2006.074997
-
Chan KCA, Ding CM, Gerovassili A, et al. Hypermethylated RASSF1A in maternal plasma: A universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis. Clin Chem 2006; 52: 2211-8. (Pubitemid 44924994)
-
(2006)
Clinical Chemistry
, vol.52
, Issue.12
, pp. 2211-2218
-
-
Chan, K.C.A.1
Ding, C.2
Gerovassili, A.3
Yeung, S.W.4
Chiu, R.W.K.5
Leung, T.N.6
Lau, T.K.7
Chim, S.S.C.8
Chung, G.T.Y.9
Nicolaides, K.H.10
Lo, Y.M.D.11
-
10
-
-
26844478953
-
Detection of the placental epigenetic signature of the maspin gene in maternal plasma
-
DOI 10.1073/pnas.0503335102
-
Chim SSC, Tong YK, Chiu RWK, et al. Detection of the placental epigenetic signature of the maspin gene in maternal plasma. Proc Natl Acad Sci USA 2005; 102: 14753-8. (Pubitemid 41457128)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.41
, pp. 14753-14758
-
-
Chim, S.S.C.1
Tong, Y.K.2
Chiu, R.W.K.3
Lau, T.K.4
Leung, T.N.5
Chan, L.Y.S.6
Oudejans, C.B.M.7
Ding, C.8
Lo, Y.M.D.9
-
11
-
-
34247843101
-
Hypermethylation of RASSF1A in human and rhesus placentas
-
DOI 10.2353/ajpath.2007.060641
-
Chiu RWK, Chim SSC, Wong IHN, et al. Hypermethylation of RASSF1A in human and rhesus placentas. Am J Pathol 2007; 170: 941-50. (Pubitemid 47339363)
-
(2007)
American Journal of Pathology
, vol.170
, Issue.3
, pp. 941-950
-
-
Chiu, R.W.K.1
Chim, S.S.C.2
Wong, I.H.N.3
Wong, C.S.C.4
Lee, W.-S.5
To, K.F.6
Tong, J.H.M.7
Yuen, R.K.C.8
Shum, A.S.W.9
Chan, J.K.C.10
Chan, L.Y.S.11
Yuen, J.W.F.12
Tong, Y.K.13
Weier, J.F.14
Ferlatte, C.15
Leung, T.N.16
Lau, T.K.17
Lo, K.W.18
Lo, Y.M.D.19
-
12
-
-
1542501831
-
Circulating cell-free fetal DNA in maternal serum appears to originate from cyto- and syncytio-trophoblastic cells. Case report
-
DOI 10.1093/humrep/deh117
-
Flori E, Doray B, Gautier E, et al. Circulating cell-free fetal DNA in maternal serum appears to originate from cyto- and syncytio-trophoblastic cells. Case report. Hum Reprod 2004; 19: 723-4. (Pubitemid 38344540)
-
(2004)
Human Reproduction
, vol.19
, Issue.3
, pp. 723-724
-
-
Flori, E.1
Doray, B.2
Gautier, E.3
Kohler, M.4
Ernault, P.5
Flori, J.6
Costa, J.M.7
-
13
-
-
0346458745
-
Earliest gestational age for fetal sexing in cell-free maternal plasma
-
DOI 10.1002/pd.750
-
Rijnders RJP, Van der Luijt RB, Peters EDJ, et al. Earliest gestational age for fetal sexing in cell-free maternal plasma. Prenat Diagn 2003; 23: 1042-4. (Pubitemid 38084143)
-
(2003)
Prenatal Diagnosis
, vol.23
, Issue.13
, pp. 1042-1044
-
-
Rijnders, R.J.P.1
Van Der Luijt, R.B.2
Peters, E.D.J.3
Goeree, J.K.4
Van Der Schoot, C.E.5
Ploos Van Amstel, J.K.6
Christiaens, G.C.M.L.7
-
14
-
-
54049132561
-
Microfluidics digital PCR reveals a higher than expected fraction offetal DNA inmaternal plasma
-
Lun FMF, Chiu RWK, Chan KCA, et al. Microfluidics digital PCR reveals a higher than expected fraction offetal DNA inmaternal plasma. Clin Chem 2008; 54: 1664-72.
-
(2008)
Clin Chem
, vol.54
, pp. 1664-1672
-
-
Lun, F.M.F.1
Chiu, R.W.K.2
Chan, K.C.A.3
-
15
-
-
79958087361
-
Non-invasive prenatal determination of fetal sex: Translating research into clinical practice
-
Hill M, Finning K, Martin P, et al. Non-invasive prenatal determination of fetal sex: translating research into clinical practice. Clin Genet 2010; 80: 68-75.
-
(2010)
Clin Genet
, vol.80
, pp. 68-75
-
-
Hill, M.1
Finning, K.2
Martin, P.3
-
16
-
-
0033364339
-
Rapid clearance of fetal DNA from maternal plasma
-
DOI 10.1086/302205
-
Lo YMD, Zhang J, Leung TN, et al. Rapid clearance of fetal DNA from maternal plasma. Am J Hum Genet 1999; 64: 218-24. (Pubitemid 30428975)
-
(1999)
American Journal of Human Genetics
, vol.64
, Issue.1
, pp. 218-224
-
-
Dennis Lo, Y.M.1
Zhang, J.2
Leung, T.N.3
Lau, T.K.4
Chang, A.M.Z.5
Magnus Hjelm, N.6
-
17
-
-
78650207098
-
Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus
-
Lo YMD, Chan KCA, Sun H, et al. Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus. Sci Transl Med 2010; 2: 61-91.
-
(2010)
Sci Transl Med
, vol.2
, pp. 61-91
-
-
Lo, Y.M.D.1
Chan, K.C.A.2
Sun, H.3
-
18
-
-
39149099757
-
Non-invasive fetal sex determination: Impact on clinical practice
-
Finning KM, Chitty LS. Non-invasive fetal sex determination: Impact on clinical practice. Semin Fetal Neonatal Med 2008; 13: 69-75.
-
(2008)
Semin Fetal Neonatal Med
, vol.13
, pp. 69-75
-
-
Finning, K.M.1
Chitty, L.S.2
-
19
-
-
33748787168
-
Diagnostic accuracy of noninvasive fetal Rh genotyping from maternal blood-A meta-analysis
-
DOI 10.1016/j.ajog.2006.07.033, PII S0002937806009641
-
Geifman-Holtzman O, Grotegut CA, Gaughan JP. Diagnostic accuracy of noninvasive fetal Rh genotyping from maternal blood - A meta-analysis. Am J Obstet Gynecol 2006; 195: 1163-73. (Pubitemid 44415679)
-
(2006)
American Journal of Obstetrics and Gynecology
, vol.195
, Issue.4
, pp. 1163-1173
-
-
Geifman-Holtzman, O.1
Grotegut, C.A.2
Gaughan, J.P.3
-
20
-
-
67649958254
-
Non-invasive prenatal diagnosis by single molecule counting technologies
-
Chiu RWK, Cantor CR, Lo YMD. Non-invasive prenatal diagnosis by single molecule counting technologies. Trends Genet 2009; 25: 324-331.
-
(2009)
Trends Genet
, vol.25
, pp. 324-331
-
-
Chiu, R.W.K.1
Cantor, C.R.2
Lo, Y.M.D.3
-
23
-
-
0003519583
-
-
2nd ed. Oxford: Blackwell Science
-
Daniels G. Human Blood Groups. 2nd ed. Oxford: Blackwell Science; 2002; 195-274.
-
(2002)
Human Blood Groups
, pp. 195-274
-
-
Daniels, G.1
-
24
-
-
0027216648
-
Prenatal determination of fetal RhD type by DNA amplification
-
DOI 10.1056/NEJM199308263290903
-
Bennett PR, Kim CL, Colin Y, et al. Prenatal determination of fetal RhD type by DNA amplification. N Engl J Med 1993; 329: 607-10. (Pubitemid 23244811)
-
(1993)
New England Journal of Medicine
, vol.329
, Issue.9
, pp. 607-610
-
-
Bennett, P.R.1
Le Van Kim, C.2
Colin, Y.3
Warwick, R.M.4
Cherif-Zahar, B.5
Fisk, N.M.6
Cartron, J.-P.7
-
25
-
-
0032506669
-
Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma
-
DOI 10.1056/NEJM199812103392402
-
Lo YMD, Hjelm NM, Fidler C, et al. Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma. N Engl J Med 1998; 339: 1734-8. (Pubitemid 28555431)
-
(1998)
New England Journal of Medicine
, vol.339
, Issue.24
, pp. 1734-1738
-
-
Lo, Y.M.D.1
Hjelm, N.M.2
Fidler, C.3
Sargent, I.L.4
Murphy, M.F.5
Chamberlain, P.F.6
Poon, P.M.K.7
Redman, C.W.G.8
Wainscoat, J.S.9
-
27
-
-
42249108710
-
Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immunoglobulin in RhD negative pregnant women: Prospective feasibility study
-
DOI 10.1136/bmj.39518.463206.25
-
Finning K, Martin P, Summers J, et al. Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immuno-globulin in RhD negative pregnant women: prospective feasibility study. BMJ 2008; 336: 816-8. (Pubitemid 351548224)
-
(2008)
BMJ
, vol.336
, Issue.7648
, pp. 816-818
-
-
Finning, K.1
Martin, P.2
Summers, J.3
Massey, E.4
Poole, G.5
Daniels, G.6
-
28
-
-
55349105463
-
The determination of the fetal D status from maternal plasma for decision making on Rh prophylaxis is feasible
-
Muller SP, Bartels I, Stein W, et al. The determination of the fetal D status from maternal plasma for decision making on Rh prophylaxis is feasible. Transfusion 2008; 48: 2292-301.
-
(2008)
Transfusion
, vol.48
, pp. 2292-2301
-
-
Muller, S.P.1
Bartels, I.2
Stein, W.3
-
29
-
-
65549088923
-
The SAFE project: Towards non-invasive prenatal diagnosis
-
Maddocks DG, Alberry MS, Attilakos G, et al. The SAFE project: towards non-invasive prenatal diagnosis. Biochem Soc Trans 2009; 37: 460-5.
-
(2009)
Biochem Soc Trans
, vol.37
, pp. 460-465
-
-
Maddocks, D.G.1
Alberry, M.S.2
Attilakos, G.3
-
30
-
-
10344242623
-
Real time PCR of bi-allelic insertion/deletion polymorphisms can serve as a reliable positive control for cell-free fetal DNA in non-invasive prenatal genotyping
-
Van der Schoot CE, Rijnders RJP, Bossers B, et al. Real time PCR of bi-allelic insertion/deletion polymorphisms can serve as a reliable positive control for cell-free fetal DNA in non-invasive prenatal genotyping. Blood 2003; 102: 315.
-
(2003)
Blood
, vol.102
, pp. 315
-
-
Van Der Schoot, C.E.1
Rijnders, R.J.P.2
Bossers, B.3
-
32
-
-
0033037877
-
The sonographic identification of fetal gender from 11 to 14 weeks of gestation
-
DOI 10.1046/j.1469-0705.1999.13050301.x
-
Whitlow BJ, Lazanakis MS, Economides DL. The sonographic identification of fetal gender from 11 to 14 weeks of gestation. Ultrasound Obstet Gynecol 1999; 13: 301-4. (Pubitemid 29312635)
-
(1999)
Ultrasound in Obstetrics and Gynecology
, vol.13
, Issue.5
, pp. 301-304
-
-
Whitlow, B.J.1
Lazanakis, M.S.2
Economides, D.L.3
-
33
-
-
0030848048
-
Morphogenesis of the human external male genitalia
-
DOI 10.1007/s003830050162
-
Ammini AC, Sabherwal U, Mukhopadhyay C, et al. Morphogenesis of the human external male genitalia. Pediatr Surg Int 1997; 12: 401-406. (Pubitemid 27322816)
-
(1997)
Pediatric Surgery International
, vol.12
, Issue.5-6
, pp. 401-406
-
-
Ammini, A.C.1
Sabherwal, U.2
Mukhopadhyay, C.3
Vijayaraghavan, M.4
Pandey, J.5
-
35
-
-
33750731763
-
The obstetric and gynaecological management of women with inherited bleeding disorders - Review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors' Organization
-
Lee CA, Chi C, Pavord SR, et al. The obstetric and gynaecological management of women with inherited bleeding disorders - review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors' Organization. Haemophilia 2006; 12: 301-36.
-
(2006)
Haemophilia
, vol.12
, pp. 301-336
-
-
Lee, C.A.1
Chi, C.2
Pavord, S.R.3
-
36
-
-
0037046654
-
New strategy for prenatal diagnosis of X-linked disorders [6] (multiple letters)
-
DOI 10.1056/NEJM200205093461918
-
Costa JM, Benachi A, Gautier E. New strategy for prenatal diagnosis of X-linked disorders. N Engl J Med 2002; 346: 1502. (Pubitemid 34755726)
-
(2002)
New England Journal of Medicine
, vol.346
, Issue.19
, pp. 1502
-
-
Costa, J.-M.1
Benachi, A.2
Gautier, E.3
-
37
-
-
29544450593
-
Reduction in diagnostic and therapeutic interventions by non-invasive determination of fetal sex in early pregnancy
-
DOI 10.1002/pd.1284
-
Hyett JA, Gardener G, Stojilkovic-Mikic T, et al. Reduction in diagnostic and therapeutic interventions by non-invasive determination of fetal sex in early pregnancy. Prenat Diagn 2005; 25: 1111-6. (Pubitemid 43016291)
-
(2005)
Prenatal Diagnosis
, vol.25
, Issue.12
, pp. 1111-1116
-
-
Hyett, J.A.1
Gardener, G.2
Stojilkovic-Mikic, T.3
Finning, K.M.4
Martin, P.G.5
Rodeck, C.H.6
Chitty, L.S.7
-
38
-
-
33847239357
-
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia
-
Santacroce R, Vecchione G, Tomaiyolo M, et al. Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia. Haemophilia 2006; 12: 417-22.
-
(2006)
Haemophilia
, vol.12
, pp. 417-422
-
-
Santacroce, R.1
Vecchione, G.2
Tomaiyolo, M.3
-
39
-
-
20444462824
-
Congenital adrenal hyperplasia
-
DOI 10.1016/S0140-6736(05)66736-0, PII S0140673605667360
-
Merke DP, Bornstein SR. Congenital adrenal hyperplasia. Lancet 2005; 365: 2125-36. (Pubitemid 40826971)
-
(2005)
Lancet
, vol.365
, Issue.9477
, pp. 2125-2136
-
-
Merke, D.P.1
Bornstein, S.R.2
-
40
-
-
77956588420
-
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline
-
Speiser PW, Azziz R, Baskin LS, et al. Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab 2010; 95: 4133-60.
-
(2010)
J Clin Endocrinol Metab
, vol.95
, pp. 4133-4160
-
-
Speiser, P.W.1
Azziz, R.2
Baskin, L.S.3
-
41
-
-
59649095981
-
Prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
-
Nimkarn S, New MI. Prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Mol Cell Endocrinol 2009; 300: 192-6.
-
(2009)
Mol Cell Endocrinol
, vol.300
, pp. 192-196
-
-
Nimkarn, S.1
New, M.I.2
-
42
-
-
0037622188
-
Fetal sex determination from maternal blood at 6 weeks of gestation when at risk for 21-hydroxylase deficiency
-
DOI 10.1016/S0029-7844(03)00064-4
-
Bartha JL, Finning K, Soothill PW. Fetal sex determination from maternal blood at 6 weeks of gestation when at risk for 21-hydroxylase deficiency. Obstet Gynecol 2003; 101: 1135-6. (Pubitemid 36566404)
-
(2003)
Obstetrics and Gynecology
, vol.101
, Issue.SUPPL. 5
, pp. 1135-1136
-
-
Bartha, J.L.1
Finning, K.2
Soothill, P.W.3
-
43
-
-
79952230961
-
Incremental cost of non-invasive prenatal diagnosis versus invasive prenatal diagnosis of fetal sex in England
-
Hill M, Taffinder S, Chitty LS, Morris S. Incremental cost of non-invasive prenatal diagnosis versus invasive prenatal diagnosis of fetal sex in England. Prenat Diagn 2011; 31: 267-73.
-
(2011)
Prenat Diagn
, vol.31
, pp. 267-273
-
-
Hill, M.1
Taffinder, S.2
Chitty, L.S.3
Morris, S.4
-
44
-
-
33845942655
-
ACOG Practice Bulletin No. 77: Screening for fetal chromosomal abnormalities
-
ACOG Committee on Practice Bulletins
-
ACOG Committee on Practice Bulletins. ACOG Practice Bulletin No. 77: screening for fetal chromosomal abnormalities. Obstet Gynecol 2007; 109: 217-227.
-
(2007)
Obstet Gynecol
, vol.109
, pp. 217-227
-
-
-
45
-
-
33846903851
-
Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection
-
Lo YMD, Tsui NBY, Chiu RWK, et al. Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection. Nat Med 2007; 13: 218-23.
-
(2007)
Nat Med
, vol.13
, pp. 218-223
-
-
Lo, Y.M.D.1
Tsui, N.B.Y.2
Chiu, R.W.K.3
-
46
-
-
33845522324
-
Noninvasive prenatal detection of fetal trisomy 18 by epigenetic allelic ratio analysis in maternal plasma: Theoretical and empirical considerations
-
DOI 10.1373/clinchem.2006.076851
-
Tong YK, Ding CM, Chiu RWK, et al. Noninvasive prenatal detection of fetal trisomy 18 by epigenetic allelic ratio analysis in maternal plasma: Theoretical and empirical considerations. Clin Chem 2006; 52: 2194-202. (Pubitemid 44924992)
-
(2006)
Clinical Chemistry
, vol.52
, Issue.12
, pp. 2194-2202
-
-
Tong, Y.K.1
Ding, C.2
Chiu, R.W.K.3
Gerovassili, A.4
Chim, S.S.C.5
Leung, T.Y.6
Leung, T.N.7
Lau, T.K.8
Nicolaides, K.H.9
Lo, Y.M.D.10
-
47
-
-
73449106855
-
Noninvasive prenatal detection of trisomy 21 by an epigenetic-genetic chromosome-dosage approach
-
Tong YK, Jin SN, Chiu RWK, et al. Noninvasive prenatal detection of trisomy 21 by an epigenetic-genetic chromosome-dosage approach. Clin Chem 2010; 56: 90-8.
-
(2010)
Clin Chem
, vol.56
, pp. 90-98
-
-
Tong, Y.K.1
Jin, S.N.2
Chiu, R.W.K.3
-
48
-
-
73449090473
-
Synergy of total PLAC4 RNA concentration and measurement of the RNA single-nucleotide polymorphism allelic ratio for the noninvasive prenatal detection of trisomy 21
-
Tsui NBY, Akolekar R, Chiu RWK, et al. Synergy of total PLAC4 RNA concentration and measurement of the RNA single-nucleotide polymorphism allelic ratio for the noninvasive prenatal detection of trisomy 21. Clin Chem 2010; 56: 73-81.
-
(2010)
Clin Chem
, vol.56
, pp. 73-81
-
-
Tsui, N.B.Y.1
Akolekar, R.2
Chiu, R.W.K.3
-
49
-
-
0036151029
-
Novel real-time quantitative PCR test for trisomy 21
-
Zimmermann B, Holzgreve W, Wenzel F, et al. Novel real-time quantitative PCR test for trisomy 21. Clin Chem 2002; 48: 362-3. (Pubitemid 34107277)
-
(2002)
Clinical Chemistry
, vol.48
, Issue.2
, pp. 362-363
-
-
Zimmermann, B.1
Holzgreve, W.2
Wenzel, F.3
Hahn, S.4
-
50
-
-
34548727890
-
Digital PCR for the molecular detection of fetal chromosomal aneuploidy
-
DOI 10.1073/pnas.0705765104
-
Lo YMD, Lun FMF, Chan KCA, et al. Digital PCR for the molecular detection of fetal chromosomal aneuploidy. Proc Natl Acad Sci USA 2007; 104: 13116-21. (Pubitemid 351737602)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.32
, pp. 13116-13121
-
-
Lo, Y.M.D.1
Lun, F.M.F.2
Chan, K.C.A.3
Tsui, N.B.Y.4
Chong, K.C.5
Lau, T.K.6
Leung, T.Y.7
Zee, B.C.Y.8
Cantor, C.R.9
Chiu, R.W.K.10
-
51
-
-
58149490683
-
Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNAin maternal plasma
-
Chiu RWK, Chan KCA, Gao Y, et al. Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNAin maternal plasma. Proc Natl Acad Sci USA 2008; 105: 20458-63.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 20458-20463
-
-
Chiu, R.W.K.1
Chan, K.C.A.2
Gao, Y.3
-
52
-
-
77649208031
-
Maternal plasma DNA analysis with massively parallel sequencing by ligation for noninvasive prenatal diagnosis of trisomy 21
-
Chiu RWK, Sun H, Akolekar R, et al. Maternal plasma DNA analysis with massively parallel sequencing by ligation for noninvasive prenatal diagnosis of trisomy 21. Clin Chem 2010; 56: 459-63.
-
(2010)
Clin Chem
, vol.56
, pp. 459-463
-
-
Chiu, R.W.K.1
Sun, H.2
Akolekar, R.3
-
53
-
-
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 USA 2008; 105: 16266-71.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 16266-16271
-
-
Fan, H.C.1
Blumenfeld, Y.J.2
Chitkara, U.3
-
54
-
-
78751683468
-
Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: Large scale validity study
-
Chiu RWK, Akolekar R, Zheng YWL, et al. Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study. BMJ 2011; 342: c7401.
-
(2011)
BMJ
, vol.342
-
-
Chiu, R.W.K.1
Akolekar, R.2
Zheng, Y.W.L.3
-
55
-
-
79952302397
-
Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: A study in a clinical setting
-
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: 205 e1-205 e11.
-
(2011)
Am J Obstet Gynecol
, vol.204
-
-
Ehrich, M.1
Deciu, C.2
Zwiefelhofer, T.3
-
57
-
-
79959937504
-
Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing
-
Chen EZ, Chiu RWK, Sun H, et al. Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing. PLoS One 2011; 6: e21791.
-
(2011)
PLoS One
, vol.6
-
-
Chen, E.Z.1
Chiu, R.W.K.2
Sun, H.3
|