-
1
-
-
0002232454
-
Prenatal diagnosis of chromosomal abnormalities through amniocentesis
-
Milunsky A (ed). Baltimore: Johns Hopkins University Press
-
Hsu LYF. Prenatal diagnosis of chromosomal abnormalities through amniocentesis. In: Milunsky A (ed). Genetic disorders of the fetus: Diagnosis, prevention and treatment, 3rd ed. Baltimore: Johns Hopkins University Press, 1992, pp 155-210.
-
(1992)
Genetic Disorders of the Fetus: Diagnosis, Prevention and Treatment, 3rd Ed.
, pp. 155-210
-
-
Hsu, L.Y.F.1
-
2
-
-
0021821587
-
A sonographic sign for the detection in the second trimester of the fetus with Down syndrome
-
Benacerraf BR, Barss VA, Laboda LA. A sonographic sign for the detection in the second trimester of the fetus with Down syndrome. Am J Obstet Gynecol 1985;151:1078-1079.
-
(1985)
Am J Obstet Gynecol
, vol.151
, pp. 1078-1079
-
-
Benacerraf, B.R.1
Barss, V.A.2
Laboda, L.A.3
-
3
-
-
0030075705
-
The second trimester fetus with Down syndrome; detection using sonographic features
-
Benacerraf BR. The second trimester fetus with Down syndrome; detection using sonographic features. Ultrasound Obstet Gynecol 1996;7:147-155.
-
(1996)
Ultrasound Obstet Gynecol
, vol.7
, pp. 147-155
-
-
Benacerraf, B.R.1
-
4
-
-
0023637461
-
Soft tissue nuchal fold in the second trimester fetus: Standards for normal measurements compared to the fetus with Down syndrome
-
Benacerraf BR, Frigoletto FD. Soft tissue nuchal fold in the second trimester fetus: Standards for normal measurements compared to the fetus with Down syndrome. Am J Obstet Gynecol 1987;157:1146-1149.
-
(1987)
Am J Obstet Gynecol
, vol.157
, pp. 1146-1149
-
-
Benacerraf, B.R.1
Frigoletto, F.D.2
-
5
-
-
0021247504
-
An association between low maternal serum alpha-fetoprotein and fetal chromosomal abnormalities
-
Merkatz IR, Nitkowski HM, Macri JN et al. An association between low maternal serum alpha-fetoprotein and fetal chromosomal abnormalities. Am J Obstet Gynecol 1984;148:886-894.
-
(1984)
Am J Obstet Gynecol
, vol.148
, pp. 886-894
-
-
Merkatz, I.R.1
Nitkowski, H.M.2
Macri, J.N.3
-
6
-
-
0023639762
-
Abnormal maternal serum human chorionic gonadotropin levels in pregnancies with fetal chromosome abnormalities
-
Bogart HM, Pandian MR, Jones OW. Abnormal maternal serum human chorionic gonadotropin levels in pregnancies with fetal chromosome abnormalities. Prenat Diagn 1987;7:623-630.
-
(1987)
Prenat Diagn
, vol.7
, pp. 623-630
-
-
Bogart, H.M.1
Pandian, M.R.2
Jones, O.W.3
-
7
-
-
0024354901
-
First trimester and early second trimester diagnosis of nuchal cystic hygroma by transvaginal sonography: Diverse prognosis of the septated from the non-septated lesion
-
Bronshtein M, Rottem S, Yoffe N et al. First trimester and early second trimester diagnosis of nuchal cystic hygroma by transvaginal sonography: Diverse prognosis of the septated from the non-septated lesion. Am J Obstet Gynecol 1989;161:78-82.
-
(1989)
Am J Obstet Gynecol
, vol.161
, pp. 78-82
-
-
Bronshtein, M.1
Rottem, S.2
Yoffe, N.3
-
8
-
-
0025092646
-
Diagnosis and significance of cystic hygroma in the first trimester
-
Cullen MT, Gabrielli S, Green JJ et al. Diagnosis and significance of cystic hygroma in the first trimester. Prenat Diagn 1990;10:643-651.
-
(1990)
Prenat Diagn
, vol.10
, pp. 643-651
-
-
Cullen, M.T.1
Gabrielli, S.2
Green, J.J.3
-
9
-
-
84989152502
-
First trimester diagnosis of nuchal anomalies: Significance and fetal outcome
-
Ville Y, Lalondrelle C, Doumerc S et al. First trimester diagnosis of nuchal anomalies: Significance and fetal outcome. Ultrasound Obstet Gynecol 1992;2:314-316.
-
(1992)
Ultrasound Obstet Gynecol
, vol.2
, pp. 314-316
-
-
Ville, Y.1
Lalondrelle, C.2
Doumerc, S.3
-
10
-
-
0026750114
-
High frequency of cytogenetic abnormalities in fetuses with cystic hygroma diagnosed in the first trimester
-
Shulman LP, Emerson DS, Felker RE et al. High frequency of cytogenetic abnormalities in fetuses with cystic hygroma diagnosed in the first trimester. Obstet Gynecol 1992;80:80-2.
-
(1992)
Obstet Gynecol
, vol.80
, pp. 80-82
-
-
Shulman, L.P.1
Emerson, D.S.2
Felker, R.E.3
-
11
-
-
0026562612
-
Fetal nuchal translucency; ultrasound screening for chromosomal defects in first trimester of pregnancy
-
Nicholaides KH, Azar G, Bryne D et al. Fetal nuchal translucency; ultrasound screening for chromosomal defects in first trimester of pregnancy. Br Med J 1992;304:867-869.
-
(1992)
Br Med J
, vol.304
, pp. 867-869
-
-
Nicholaides, K.H.1
Azar, G.2
Bryne, D.3
-
12
-
-
0026650003
-
First trimester diagnosis of cystic hygroma - Course and outcome
-
Van Zalen-Sprock MM, Van Vugt JMG et al. First trimester diagnosis of cystic hygroma - Course and outcome. Am J Obstet Gynecol 1992;167:94-98.
-
(1992)
Am J Obstet Gynecol
, vol.167
, pp. 94-98
-
-
Van Zalen-Sprock, M.M.1
Van Vugt, J.M.G.2
-
13
-
-
0027270381
-
Ultrasound screening for chromosomal abnormalities in the first trimester of pregnancy
-
Savoldelli G, Binkert F, Achermann J et al. Ultrasound screening for chromosomal abnormalities in the first trimester of pregnancy. Prenat Diagn 1993;13:513-518.
-
(1993)
Prenat Diagn
, vol.13
, pp. 513-518
-
-
Savoldelli, G.1
Binkert, F.2
Achermann, J.3
-
15
-
-
0027231799
-
Nuchal thickening or cystic hygromas in first- and early second- trimester fetuses: Prognosis and outcome
-
Nadel A, Bromley B, Benacerraf BR. Nuchal thickening or cystic hygromas in first-and early second-trimester fetuses: Prognosis and outcome. Obstet Gynecol 1993;82:43-48.
-
(1993)
Obstet Gynecol
, vol.82
, pp. 43-48
-
-
Nadel, A.1
Bromley, B.2
Benacerraf, B.R.3
-
16
-
-
0028111417
-
Fetal nuchal translucency thickness and risk for trisomies
-
Pandya PP, Brizot ML, Snijders RJM. Fetal nuchal translucency thickness and risk for trisomies. Obstet Gynecol 1994; 84:420-423.
-
(1994)
Obstet Gynecol
, vol.84
, pp. 420-423
-
-
Pandya, P.P.1
Brizot, M.L.2
Snijders, R.J.M.3
-
17
-
-
0028133546
-
Fetal nuchal translucency; ultrasound screening for fetal trisomy in the first trimester of pregnancy
-
Nicolaides KH, Brizot ML, Snijders RJM. Fetal nuchal translucency; ultrasound screening for fetal trisomy in the first trimester of pregnancy. Br J Obstet Gynaecol 1994;101:782-786.
-
(1994)
Br J Obstet Gynaecol
, vol.101
, pp. 782-786
-
-
Nicolaides, K.H.1
Brizot, M.L.2
Snijders, R.J.M.3
-
19
-
-
0029201492
-
First trimester Down syndrome screening using nuchal translucency: A prospective study in patients undergoing chorionic villus sampling
-
Brambati B, Cislaghi C, Tului L et al. First trimester Down syndrome screening using nuchal translucency: A prospective study in patients undergoing chorionic villus sampling. Ultrasound Obstet Gynecol 1995;5:9-14.
-
(1995)
Ultrasound Obstet Gynecol
, vol.5
, pp. 9-14
-
-
Brambati, B.1
Cislaghi, C.2
Tului, L.3
-
20
-
-
0029180678
-
Chromosomal defects and outcome in 1015 fetuses with increased nuchal translucency
-
Pandya PP, Kondylios A, Hilbert L et al. Chromosomal defects and outcome in 1015 fetuses with increased nuchal translucency. Ultrasound Obstet Gynecol 1995;5:15-19.
-
(1995)
Ultrasound Obstet Gynecol
, vol.5
, pp. 15-19
-
-
Pandya, P.P.1
Kondylios, A.2
Hilbert, L.3
-
22
-
-
0029914345
-
First trimester translucency: Aneuploidy, sonographic findings, and maternal age
-
Mahieu-Caputo D, Dommergues M, Morichon-Delvallez N et al. First trimester translucency: Aneuploidy, sonographic findings, and maternal age. Fetal Diagn Ther 1996;11:199-204.
-
(1996)
Fetal Diagn Ther
, vol.11
, pp. 199-204
-
-
Mahieu-Caputo, D.1
Dommergues, M.2
Morichon-Delvallez, N.3
-
23
-
-
0029588613
-
Screening for fetal trisomies by maternal age and fetal nuchal translucency thickness at 10 to 14 weeks of gestation
-
Pandya PP, Snijders RJM, Johnson SP et al. Screening for fetal trisomies by maternal age and fetal nuchal translucency thickness at 10 to 14 weeks of gestation. Br J Obstet Gynaecol 1995;102:957-962.
-
(1995)
Br J Obstet Gynaecol
, vol.102
, pp. 957-962
-
-
Pandya, P.P.1
Snijders, R.J.M.2
Johnson, S.P.3
-
24
-
-
0029114144
-
Nuchal translucency thickness and crown-rump length in twin pregnancies with chromosomally abnormal fetuses
-
Pandya PP, Hilbert F, Snijders RJM et al. Nuchal translucency thickness and crown-rump length in twin pregnancies with chromosomally abnormal fetuses. J Ultrasound Med 1995;14: 565-568.
-
(1995)
J Ultrasound Med
, vol.14
, pp. 565-568
-
-
Pandya, P.P.1
Hilbert, F.2
Snijders, R.J.M.3
-
25
-
-
0028849426
-
Maternal age and gestational age specific risk for chromosomal defects
-
Snijders RJM, Sebire NJ, Souka A et al. Maternal age and gestational age specific risk for chromosomal defects. Fetal Diagn Ther 1995;10:356-367.
-
(1995)
Fetal Diagn Ther
, vol.10
, pp. 356-367
-
-
Snijders, R.J.M.1
Sebire, N.J.2
Souka, A.3
-
26
-
-
0030075767
-
Intrauterine lethality of trisomy 21 fetuses with increased nuchal translucency thickness
-
Hyett JA, Sebire NJ, Snijders RJM et al. Intrauterine lethality of trisomy 21 fetuses with increased nuchal translucency thickness. Ultrasound Obstet Gynecol 1996;7:101-103.
-
(1996)
Ultrasound Obstet Gynecol
, vol.7
, pp. 101-103
-
-
Hyett, J.A.1
Sebire, N.J.2
Snijders, R.J.M.3
-
27
-
-
0029065027
-
First trimester nuchal translucency and cardiac septal defects in fetuses with trisomy 21
-
Hyett JA, Mosoco G, Nicolaides KH. First trimester nuchal translucency and cardiac septal defects in fetuses with trisomy 21. Am J Obstet Gynecol 1995;172:1411-1413.
-
(1995)
Am J Obstet Gynecol
, vol.172
, pp. 1411-1413
-
-
Hyett, J.A.1
Mosoco, G.2
Nicolaides, K.H.3
-
28
-
-
0028863134
-
Increased nuchal translucency in trisomy 21 fetuses; relation to narrowing of the aortic isthmus
-
Hyett JA, Mosoco G, Nicolaides KH. Increased nuchal translucency in trisomy 21 fetuses; relation to narrowing of the aortic isthmus. Hum Reprod 1995;10:3049-3051.
-
(1995)
Hum Reprod
, vol.10
, pp. 3049-3051
-
-
Hyett, J.A.1
Mosoco, G.2
Nicolaides, K.H.3
-
29
-
-
0029319741
-
Natural history of trisomy 21 fetuses with increased nuchal translucency thickness
-
Pandya PP, Snijders RJM, Johnson SP et al. Natural history of trisomy 21 fetuses with increased nuchal translucency thickness. Ultrasound Obstet Gynecol 1995;5:381-383.
-
(1995)
Ultrasound Obstet Gynecol
, vol.5
, pp. 381-383
-
-
Pandya, P.P.1
Snijders, R.J.M.2
Johnson, S.P.3
-
30
-
-
0030122566
-
Fetal heart rate in trisomy 21 and other chromosomal abnormalities at 10 to 14 weeks of gestation
-
Hyett JA, Noble PL, Snijders RJM et al. Fetal heart rate in trisomy 21 and other chromosomal abnormalities at 10 to 14 weeks of gestation. Ultrasound Obstet Gynecol 1996;7:239-244.
-
(1996)
Ultrasound Obstet Gynecol
, vol.7
, pp. 239-244
-
-
Hyett, J.A.1
Noble, P.L.2
Snijders, R.J.M.3
-
31
-
-
0027962426
-
Maternal serum pregnancy associated placental protein a (PAPP-A) and fetal nuchal translucency thickness for the prediction of fetal trisomies in the first trimester of pregnancy
-
Brizot ML, Snijders RJM, Bersinger NA et al. Maternal serum pregnancy associated placental protein A (PAPP-A) and fetal nuchal translucency thickness for the prediction of fetal trisomies in the first trimester of pregnancy. Obstet Gynecol 1994;84:918-922.
-
(1994)
Obstet Gynecol
, vol.84
, pp. 918-922
-
-
Brizot, M.L.1
Snijders, R.J.M.2
Bersinger, N.A.3
-
32
-
-
0028929622
-
Maternal serum hCG and fetal nuchal translucency thickness for the prediction of fetal trisomies in the first trimester of pregnancy
-
Brizot ML, Snijders RJM, Butler J et al. Maternal serum hCG and fetal nuchal translucency thickness for the prediction of fetal trisomies in the first trimester of pregnancy. Br J Obstet Gynaecol 1995;102:127-132.
-
(1995)
Br J Obstet Gynaecol
, vol.102
, pp. 127-132
-
-
Brizot, M.L.1
Snijders, R.J.M.2
Butler, J.3
-
33
-
-
0029421091
-
Screening for fetal trisomy 21 in the first trimester of pregnancy: Maternal serum free β-hCG and fetal nuchal translucency thickness
-
Noble PL, Abraham HD, Snijders RJM et al. Screening for fetal trisomy 21 in the first trimester of pregnancy: Maternal serum free β-hCG and fetal nuchal translucency thickness. Ultrasound Obstet Gynecol 1995;6:390-395.
-
(1995)
Ultrasound Obstet Gynecol
, vol.6
, pp. 390-395
-
-
Noble, P.L.1
Abraham, H.D.2
Snijders, R.J.M.3
-
34
-
-
0029181608
-
The implementation of first trimester scanning at 10 to 13 weeks gestation and the measurement of fetal nuchal translucency thickness in two maternity units
-
Pandya PP, Goldberg H, Walton B et al. The implementation of first trimester scanning at 10 to 13 weeks gestation and the measurement of fetal nuchal translucency thickness in two maternity units. Ultrasound Obstet Gynecol 1995;5:20-25.
-
(1995)
Ultrasound Obstet Gynecol
, vol.5
, pp. 20-25
-
-
Pandya, P.P.1
Goldberg, H.2
Walton, B.3
-
35
-
-
0029002236
-
First trimester fetal nuchal translucency: Problems with screening the general population
-
Roberts LJ, Bewley S, Mackinson AM et al. First trimester fetal nuchal translucency: Problems with screening the general population. Br J 1995;102:381-385.
-
(1995)
Br J
, vol.102
, pp. 381-385
-
-
Roberts, L.J.1
Bewley, S.2
Mackinson, A.M.3
-
36
-
-
0029030338
-
First trimester fetal nuchal translucency: Problems with screening the general population 2
-
Bewley S, Roberts LJ, Mackinson AM et al. First trimester fetal nuchal translucency: Problems with screening the general population 2. Br J Obstet Gynaecol 1995;102:386-388.
-
(1995)
Br J Obstet Gynaecol
, vol.102
, pp. 386-388
-
-
Bewley, S.1
Roberts, L.J.2
Mackinson, A.M.3
-
38
-
-
0024524531
-
First trimester growth delay in trisomy 18
-
Lynch L, Berkowitz RL. First trimester growth delay in trisomy 18. Am J Perinatol 1989;6:237-239.
-
(1989)
Am J Perinatol
, vol.6
, pp. 237-239
-
-
Lynch, L.1
Berkowitz, R.L.2
-
39
-
-
0028955573
-
Crown-rump length in chromosomally abnormal fetuses at 10 to 13 weeks' gestation
-
Kuhn P, Brizot ML, Pandya PP et al. Crown-rump length in chromosomally abnormal fetuses at 10 to 13 weeks' gestation. Am J Obstet Gynecol 1995;172:32-35.
-
(1995)
Am J Obstet Gynecol
, vol.172
, pp. 32-35
-
-
Kuhn, P.1
Brizot, M.L.2
Pandya, P.P.3
-
40
-
-
0026618875
-
The smaller than expected first trimester fetus is at increased risk for chromosome anomalies
-
Drugan A, Johnson MP, Isada NB et al. The smaller than expected first trimester fetus is at increased risk for chromosome anomalies. Am J Obstet Gynecol 1992;167:1525-1528.
-
(1992)
Am J Obstet Gynecol
, vol.167
, pp. 1525-1528
-
-
Drugan, A.1
Johnson, M.P.2
Isada, N.B.3
-
41
-
-
0027285015
-
Biparietal diameter and crown-rump length in fetuses with Down's syndrome: Implications for antenatal serum screening for Down's syndrome
-
Wald NJ, Smith D, Kennard A et al. Biparietal diameter and crown-rump length in fetuses with Down's syndrome: Implications for antenatal serum screening for Down's syndrome. Br J Obstet Gynaecol 1993;100:430-435.
-
(1993)
Br J Obstet Gynaecol
, vol.100
, pp. 430-435
-
-
Wald, N.J.1
Smith, D.2
Kennard, A.3
-
42
-
-
0026734312
-
Early growth retardation in the first trimester: Is it characteristic of the chromosomally abnormal fetus
-
Leelapatana P, Garrett WJ, Warren PS. Early growth retardation in the first trimester: Is it characteristic of the chromosomally abnormal fetus. Aust NZ J Obstet Gynaecol 1992;32: 95-97.
-
(1992)
Aust NZ J Obstet Gynaecol
, vol.32
, pp. 95-97
-
-
Leelapatana, P.1
Garrett, W.J.2
Warren, P.S.3
-
43
-
-
0026094675
-
Ultrasound and genetic features of a term triploid pregnancy
-
Wasserman SA, Bofinger MK, Saldana LR. Ultrasound and genetic features of a term triploid pregnancy. Am J Perinatol 1991;8:398-401.
-
(1991)
Am J Perinatol
, vol.8
, pp. 398-401
-
-
Wasserman, S.A.1
Bofinger, M.K.2
Saldana, L.R.3
-
44
-
-
0023906451
-
Intrauterine growth retardation in the first trimester associated with triploidy
-
Benacerraf BR. Intrauterine growth retardation in the first trimester associated with triploidy. J Ultrasound Med 1988;7: 153-154.
-
(1988)
J Ultrasound Med
, vol.7
, pp. 153-154
-
-
Benacerraf, B.R.1
-
45
-
-
0023639762
-
Abnormal maternal serum chorionic gonadotropin levels in pregnancies with fetal chromosome abnormalities
-
Bogart MH, Pandian MR, Jones OW. Abnormal maternal serum chorionic gonadotropin levels in pregnancies with fetal chromosome abnormalities. Prenat Diagn 1987;7:623-630.
-
(1987)
Prenat Diagn
, vol.7
, pp. 623-630
-
-
Bogart, M.H.1
Pandian, M.R.2
Jones, O.W.3
-
46
-
-
0023801407
-
Low second trimester maternal serum unconjugated estriol in pregnancies with Down's syndrome
-
Canick JA, Knight GJ, Palomaki GE et al. Low second trimester maternal serum unconjugated estriol in pregnancies with Down's syndrome. Br J Obstet Gynaecol 1988;95:330-333.
-
(1988)
Br J Obstet Gynaecol
, vol.95
, pp. 330-333
-
-
Canick, J.A.1
Knight, G.J.2
Palomaki, G.E.3
-
47
-
-
0023726523
-
Maternal serum screening for Down syndrome in early pregnancy
-
Wald NJ, Cuckle HS, Densem JW et al. Maternal serum screening for Down syndrome in early pregnancy. Br Med J 1988;297:883-887.
-
(1988)
Br Med J
, vol.297
, pp. 883-887
-
-
Wald, N.J.1
Cuckle, H.S.2
Densem, J.W.3
-
48
-
-
0029587397
-
First trimester screening for Down's syndrome
-
Wald NJ, Kennard A, Hackshaw AK. First trimester screening for Down's syndrome. Prenat Diagn 1995;15:1227-1240
-
(1995)
Prenat Diagn
, vol.15
, pp. 1227-1240
-
-
Wald, N.J.1
Kennard, A.2
Hackshaw, A.K.3
-
49
-
-
0027483421
-
Low maternal serum levels of pregnancy associated plasma protein a (PAPP-A) in the first trimester in association with abnormal fetal karyoptype
-
Brambati B, Macintosh MCM, Teisner B et al. Low maternal serum levels of pregnancy associated plasma protein A (PAPP-A) in the first trimester in association with abnormal fetal karyoptype. Br. J Obstet Gynaecol 1993;100:324-326.
-
(1993)
Br. J Obstet Gynaecol
, vol.100
, pp. 324-326
-
-
Brambati, B.1
Macintosh, M.C.M.2
Teisner, B.3
-
50
-
-
0025277434
-
First-trimester maternal serum biochemical indicators in Down syndrome
-
Brock DJH, Barron L, Halloway S et al. First-trimester maternal serum biochemical indicators in Down syndrome. Prenat Diagn 1990;10:245-251.
-
(1990)
Prenat Diagn
, vol.10
, pp. 245-251
-
-
Brock, D.J.H.1
Barron, L.2
Halloway, S.3
-
51
-
-
0025733119
-
First-trimester maternal serum alpha-fetoprotein and chorionic gonadotropin in aneuploid pregnancies
-
Johnson A, Cowchock FS, Darby M et al. First-trimester maternal serum alpha-fetoprotein and chorionic gonadotropin in aneuploid pregnancies Prenat Diagn 1991;11:443-450.
-
(1991)
Prenat Diagn
, vol.11
, pp. 443-450
-
-
Johnson, A.1
Cowchock, F.S.2
Darby, M.3
-
52
-
-
0025054692
-
First-trimester maternal serum alpha-fetoprotein and human chorionic gonadotropin screening for chromosome defects
-
Nebiolo L, Ozturk M, Brambati B et al. First-trimester maternal serum alpha-fetoprotein and human chorionic gonadotropin screening for chromosome defects. Prenat Diagn 1990;10: 575-581.
-
(1990)
Prenat Diagn
, vol.10
, pp. 575-581
-
-
Nebiolo, L.1
Ozturk, M.2
Brambati, B.3
-
53
-
-
0028050212
-
First-trimester biochemical screening for trisomy 21: The role of free beta-hCG, alpha fetoprotein and pregnancy-associated plasma protein A
-
Spencer K, Aitken DA, Crossley JA et al. First-trimester biochemical screening for trisomy 21: The role of free beta-hCG, alpha fetoprotein and pregnancy-associated plasma protein A. Ann Clin Biochem 1994;31:447-454.
-
(1994)
Ann Clin Biochem
, vol.31
, pp. 447-454
-
-
Spencer, K.1
Aitken, D.A.2
Crossley, J.A.3
-
54
-
-
0025833029
-
First trimester maternal serum unconjugated estriol and alpha-fetoprotein in fetal Down's syndrome
-
Crandall BF, Golbus M, Goldberg JD et al. First trimester maternal serum unconjugated estriol and alpha-fetoprotein in fetal Down's syndrome. Prenat Diagn 1991;11:377-380.
-
(1991)
Prenat Diagn
, vol.11
, pp. 377-380
-
-
Crandall, B.F.1
Golbus, M.2
Goldberg, J.D.3
-
55
-
-
0027297034
-
First trimester maternal serum Schwangerschafts protein 1 (SP1) in pregnancies associated with chromosomal anomalies
-
Macintosh MCM, Brambati B, Chard T et al. First trimester maternal serum Schwangerschafts protein 1 (SP1) in pregnancies associated with chromosomal anomalies. Prenat Diagn 1993;13:563-8.
-
(1993)
Prenat Diagn
, vol.13
, pp. 563-568
-
-
Macintosh, M.C.M.1
Brambati, B.2
Chard, T.3
-
56
-
-
0030027891
-
First trimester Down syndrome screening: Free β-human chorionic gonadotropin and pregnancy-associated plasma protein A
-
Krantz DA, Larsen JW, Buchanan PD et al. First trimester Down syndrome screening: Free β-human chorionic gonadotropin and pregnancy-associated plasma protein A. Am J Obstet Gynecol 1996;174:612-6.
-
(1996)
Am J Obstet Gynecol
, vol.174
, pp. 612-616
-
-
Krantz, D.A.1
Larsen, J.W.2
Buchanan, P.D.3
-
57
-
-
0028173243
-
Urinary β-core human chorionic gonadotropin; a new approach to Down's syndrome screening
-
Cuckle HS, Iles RK, Chard T. Urinary β-core human chorionic gonadotropin; a new approach to Down's syndrome screening. Prenat Diagn 1994;14:953-8.
-
(1994)
Prenat Diagn
, vol.14
, pp. 953-958
-
-
Cuckle, H.S.1
Iles, R.K.2
Chard, T.3
-
58
-
-
0027940395
-
Serum PAPP-A and free β-hCG are first trimester markers for Down syndrome
-
Brambati B, Tului L, Bonacchi I et al. Serum PAPP-A and free β-hCG are first trimester markers for Down syndrome. Prenat Diagn 1994;14:1043-7.
-
(1994)
Prenat Diagn
, vol.14
, pp. 1043-1047
-
-
Brambati, B.1
Tului, L.2
Bonacchi, I.3
-
59
-
-
0028020792
-
First trimester maternal serum alpha-fetoprotein as a marker for fetal chromosomal disorders
-
Van Lith JMM. First trimester maternal serum alpha-fetoprotein as a marker for fetal chromosomal disorders. Prenat Diagn 1994;14:963-971.
-
(1994)
Prenat Diagn
, vol.14
, pp. 963-971
-
-
Van Lith, J.M.M.1
-
60
-
-
0029011851
-
Analysis of maternal serum alpha-fetoprotein and free beta human chorionic gonadotropin in first trimester: Implications for Down's syndrome screening
-
Berry E, Aitken DA, Crossley JA et al. Analysis of maternal serum alpha-fetoprotein and free beta human chorionic gonadotropin in first trimester: implications for Down's syndrome screening. Prenat Diagn 1995;15:555-565.
-
(1995)
Prenat Diagn
, vol.15
, pp. 555-565
-
-
Berry, E.1
Aitken, D.A.2
Crossley, J.A.3
-
61
-
-
0028343821
-
Maternal serum human chorionic gonadotropin and pregnancy-associated plasma protein A, markers for fetal Down syndrome at 8 to 14 weeks
-
Macintosh MCM, Iles R, Teisner B et al. Maternal serum human chorionic gonadotropin and pregnancy-associated plasma protein A, markers for fetal Down syndrome at 8 to 14 weeks. Prenat Diagn 1994;14:203-208.
-
(1994)
Prenat Diagn
, vol.14
, pp. 203-208
-
-
Macintosh, M.C.M.1
Iles, R.2
Teisner, B.3
-
62
-
-
0028928542
-
Evaluation of maternal dimeric inhibin a as a first trimester marker of Down's syndrome
-
Wallace EM, Grant VE, Swanston IA et al. Evaluation of maternal dimeric inhibin A as a first trimester marker of Down's syndrome. Prenat Diagn 1995;15:359-362.
-
(1995)
Prenat Diagn
, vol.15
, pp. 359-362
-
-
Wallace, E.M.1
Grant, V.E.2
Swanston, I.A.3
-
63
-
-
0029869141
-
Dimeric inhibin a as a marker for Down's syndrome in early pregnancy
-
Aitken DA, Wallace EM, Crossley JA et al. Dimeric inhibin A as a marker for Down's syndrome in early pregnancy. N Engl J Med 1996;334:1231-1236.
-
(1996)
N Engl J Med
, vol.334
, pp. 1231-1236
-
-
Aitken, D.A.1
Wallace, E.M.2
Crossley, J.A.3
-
64
-
-
0029810786
-
Urinary β-core hCG screening in the first trimester
-
Cuckle HS, Canick JA, Kellner LH et al. Urinary β-core hCG screening in the first trimester. Prenat Diagn 1996;16:1057-1059.
-
(1996)
Prenat Diagn
, vol.16
, pp. 1057-1059
-
-
Cuckle, H.S.1
Canick, J.A.2
Kellner, L.H.3
-
65
-
-
0027496707
-
Isolating fetal cells from maternal blood Advances in prenatal diagnosis through molecular technology
-
Simpson JL, Elias S. Isolating fetal cells from maternal blood Advances in prenatal diagnosis through molecular technology. J Am Med Assoc 1993;270:2357-2361.
-
(1993)
J Am Med Assoc
, vol.270
, pp. 2357-2361
-
-
Simpson, J.L.1
Elias, S.2
-
66
-
-
0028065166
-
Prenatal genetic diagnosis by isolation and analysis of fetal cells circulating in maternal blood
-
Geifman-Holtzman O, Blatman RN, Bianchi DW. Prenatal genetic diagnosis by isolation and analysis of fetal cells circulating in maternal blood. Semin Perinatol 1994;18:366-375.
-
(1994)
Semin Perinatol
, vol.18
, pp. 366-375
-
-
Geifman-Holtzman, O.1
Blatman, R.N.2
Bianchi, D.W.3
-
67
-
-
0028793463
-
Non- or minimally invasive prenatal diagnostic tests on maternal blood samples or transcervical cells
-
Adinolfi M. Non-or minimally invasive prenatal diagnostic tests on maternal blood samples or transcervical cells. Prenat Diagn 1995;15:889-896.
-
(1995)
Prenat Diagn
, vol.15
, pp. 889-896
-
-
Adinolfi, M.1
-
68
-
-
0028674975
-
Isolating fetal cells in maternal circulation for prenatal diagnosis
-
Simpson JL, Elias S. Isolating fetal cells in maternal circulation for prenatal diagnosis. Prenat Diagn 1994;14:1229-1242.
-
(1994)
Prenat Diagn
, vol.14
, pp. 1229-1242
-
-
Simpson, J.L.1
Elias, S.2
-
69
-
-
0026906634
-
Breaking the blood barrier
-
Adinolfi M. Breaking the blood barrier. Nature Genet 1992;1: 316-318.
-
(1992)
Nature Genet
, vol.1
, pp. 316-318
-
-
Adinolfi, M.1
-
70
-
-
0025991932
-
On a noninvasive approach to prenatal diagnosis based on the detection of fetal nucleated cells in maternal blood samples
-
Adinolfi M. On a noninvasive approach to prenatal diagnosis based on the detection of fetal nucleated cells in maternal blood samples. Prenat Diagn 1991;11:799-804.
-
(1991)
Prenat Diagn
, vol.11
, pp. 799-804
-
-
Adinolfi, M.1
-
71
-
-
0027515693
-
Prenatal diagnosis from maternal blood: Simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting
-
Zheng YL, Carter NP, Price CM et al. Prenatal diagnosis from maternal blood: Simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting. J Med Genet 1993;30:1051-1056.
-
(1993)
J Med Genet
, vol.30
, pp. 1051-1056
-
-
Zheng, Y.L.1
Carter, N.P.2
Price, C.M.3
-
72
-
-
0027232847
-
Erythroid-specific antibodies enhance detection of fetal nucleated erythrocytes in maternal blood
-
Bianchi DW, Zickwolf GK, Yih MC et al. Erythroid-specific antibodies enhance detection of fetal nucleated erythrocytes in maternal blood. Prenat Diagn 1993;13:293-300.
-
(1993)
Prenat Diagn
, vol.13
, pp. 293-300
-
-
Bianchi, D.W.1
Zickwolf, G.K.2
Yih, M.C.3
-
73
-
-
0026327650
-
Prenatal diagnosis with fetal cells isolated from maternal blood by multiparameter flow cytometry
-
Price J, Elias S, Wachtel SS et al. Prenatal diagnosis with fetal cells isolated from maternal blood by multiparameter flow cytometry. Am J Obstet Gynecol 1991;165:1731-1737.
-
(1991)
Am J Obstet Gynecol
, vol.165
, pp. 1731-1737
-
-
Price, J.1
Elias, S.2
Wachtel, S.S.3
-
74
-
-
0027365371
-
Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescent in situ hybridization: Clinical experience with 4500 specimens
-
Ward BE, Gersen SL, Carelli MP et al. Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescent in situ hybridization: Clinical experience with 4500 specimens. Am J Hum Genet 1993;52:854-865.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 854-865
-
-
Ward, B.E.1
Gersen, S.L.2
Carelli, M.P.3
-
75
-
-
0028672513
-
Enrichment of fetal cells from maternal blood by high gradient magnetic cell sorting (double MACS) for PCR-based genetic analysis
-
Büsch J, Huber P, Pflüger E et al. Enrichment of fetal cells from maternal blood by high gradient magnetic cell sorting (double MACS) for PCR-based genetic analysis. Prenat Diagn 1994;14:1129-1140.
-
(1994)
Prenat Diagn
, vol.14
, pp. 1129-1140
-
-
Büsch, J.1
Huber, P.2
Pflüger, E.3
-
76
-
-
0027940370
-
Fetal cells in maternal blood: Determination of purity and yield by quantitative polymerase chain reaction
-
Bianchi DW, Shuber AP, DeMaria MA et al. Fetal cells in maternal blood: Determination of purity and yield by quantitative polymerase chain reaction. Am J Obstet Gynecol 1994; 171:922-926.
-
(1994)
Am J Obstet Gynecol
, vol.171
, pp. 922-926
-
-
Bianchi, D.W.1
Shuber, A.P.2
DeMaria, M.A.3
-
77
-
-
0028225503
-
Improved detection of fetal cells from maternal blood with polymerase chain reaction
-
Adkison LR, Andrews RH, Vowell NL et al. Improved detection of fetal cells from maternal blood with polymerase chain reaction. Am J Obstet Gynecol 1994;170:952-955.
-
(1994)
Am J Obstet Gynecol
, vol.170
, pp. 952-955
-
-
Adkison, L.R.1
Andrews, R.H.2
Vowell, N.L.3
-
78
-
-
0026761240
-
First trimester prenatal diagnosis of trisomy 21 in fetal cells from maternal blood
-
Elias S, Price J, Dockter M et al. First trimester prenatal diagnosis of trisomy 21 in fetal cells from maternal blood. Lancet 1992;340:1033.
-
(1992)
Lancet
, vol.340
, pp. 1033
-
-
Elias, S.1
Price, J.2
Dockter, M.3
-
79
-
-
0027080020
-
Detection of fetal cells with 47,XY +21 karyotype in maternal peripheral blood
-
Bianchi DW, Mahr A, Zickwolf GK et al. Detection of fetal cells with 47,XY +21 karyotype in maternal peripheral blood. Hum Genet 1992;90:368-370.
-
(1992)
Hum Genet
, vol.90
, pp. 368-370
-
-
Bianchi, D.W.1
Mahr, A.2
Zickwolf, G.K.3
-
80
-
-
0027770943
-
Detection of fetal trisomies 21 and 18 from maternal blood using triple gradient and magnetic cell sorting
-
Gänshirt-Ahlert DR, Borjesson-Stoll M, Burschyk A et al. Detection of fetal trisomies 21 and 18 from maternal blood using triple gradient and magnetic cell sorting. Am J Reprod Immunol 1993;30:194-201.
-
(1993)
Am J Reprod Immunol
, vol.30
, pp. 194-201
-
-
Gänshirt-Ahlert, D.R.1
Borjesson-Stoll, M.2
Burschyk, A.3
-
81
-
-
0028857091
-
Isolating fetal nucleated red blood cells from the maternal blood: The Baylor experience
-
Simpson JL, Lewis DE, Bischoff FZ et al. Isolating fetal nucleated red blood cells from the maternal blood: The Baylor experience. Prenat Diagn 1995;15:907-912.
-
(1995)
Prenat Diagn
, vol.15
, pp. 907-912
-
-
Simpson, J.L.1
De Lewis2
Bischoff, F.Z.3
-
82
-
-
0015211319
-
Use of the Y chromosome in prenatal sex determination
-
Shettles LB. Use of the Y chromosome in prenatal sex determination. Lancet 1971;230:52.
-
(1971)
Lancet
, vol.230
, pp. 52
-
-
Shettles, L.B.1
-
83
-
-
0026696950
-
Detection of fetal DNa in transcervical swabs from the first trimester of pregnancies by gene amplification: A new route to prenatal diagnosis?
-
Griffith-Jones MD, Miller D, Lilford RJ et al. Detection of fetal DNA in transcervical swabs from the first trimester of pregnancies by gene amplification: A new route to prenatal diagnosis? Br J Obstet Gynaecol 1992;99:508-511.
-
(1992)
Br J Obstet Gynaecol
, vol.99
, pp. 508-511
-
-
Griffith-Jones, M.D.1
Miller, D.2
Lilford, R.J.3
-
84
-
-
0028834887
-
Methods for the transcervical collection of fetal cells during the first trimester of pregnancy
-
Rodeck C, Tutschek B, Sherlock J et al. Methods for the transcervical collection of fetal cells during the first trimester of pregnancy. Prenat Diagn 1995;15:933-942.
-
(1995)
Prenat Diagn
, vol.15
, pp. 933-942
-
-
Rodeck, C.1
Tutschek, B.2
Sherlock, J.3
-
85
-
-
0028835112
-
Detection of fetal cells in transcervical samples and prenatal diagnosis of chromosomal abnormalities
-
Adinolfi M, Sherlock J, Tutshceck B et al.Detection of fetal cells in transcervical samples and prenatal diagnosis of chromosomal abnormalities. Prenat Diagn 1995;15:943-989.
-
(1995)
Prenat Diagn
, vol.15
, pp. 943-989
-
-
Adinolfi, M.1
Sherlock, J.2
Tutshceck, B.3
-
86
-
-
0029079024
-
Detection of trophoblast cells in transcervical samples collected by lavage or cytobrush
-
Kingdom J, Sherlock J, Roedeck C et al. Detection of trophoblast cells in transcervical samples collected by lavage or cytobrush. Obstet Gynecol 1995;86:283-288.
-
(1995)
Obstet Gynecol
, vol.86
, pp. 283-288
-
-
Kingdom, J.1
Sherlock, J.2
Roedeck, C.3
-
87
-
-
0028879503
-
Isolation of fetal cells from transcervical samples by micromanipulation: Molecular confirmation of their fetal origin and diagnosis of fetal aneuploidy
-
Tutshcek Sherlock J, Halder A et al. Isolation of fetal cells from transcervical samples by micromanipulation: Molecular confirmation of their fetal origin and diagnosis of fetal aneuploidy. Prenat Diagn 1995;15:951-960.
-
(1995)
Prenat Diagn
, vol.15
, pp. 951-960
-
-
Tutshcek Sherlock, J.1
Halder, A.2
-
88
-
-
0027209837
-
Detection of trisomy 18 and Y-derived sequences in fetal nucleated cells obtained by transcervical flushing
-
Adinolfi M, Davies A, Sharif S et al. Detection of trisomy 18 and Y-derived sequences in fetal nucleated cells obtained by transcervical flushing. Lancet 1993;342:403-404.
-
(1993)
Lancet
, vol.342
, pp. 403-404
-
-
Adinolfi, M.1
Davies, A.2
Sharif, S.3
-
89
-
-
0028834155
-
Prenatal detection of fetal RhD DNA sequences in transcervical samples
-
Adinolfi M, Sherlock J, Kemp T et al. Prenatal detection of fetal RhD DNA sequences in transcervical samples. Lancet 1995;345:318-319.
-
(1995)
Lancet
, vol.345
, pp. 318-319
-
-
Adinolfi, M.1
Sherlock, J.2
Kemp, T.3
|