-
1
-
-
0141863495
-
First-trimester screening for trisomies 21 and 18.First Trimester Maternal Serum Biochemistry and Fetal Nuchal Translucency Screening (BUN) Study Group.
-
Wapner R, Thom E, Simpson JL, Pergament E, Silver R, Filkins K, et al. First-trimester screening for trisomies 21 and 18.First Trimester Maternal Serum Biochemistry and Fetal Nuchal Translucency Screening (BUN) Study Group.N Engl J Med 2003;349:1405-13.
-
(2003)
N Engl J Med
, vol.349
, pp. 1405-13
-
-
Wapner, R.1
Thom, E.2
Simpson, J.L.3
Pergament, E.4
Silver, R.5
Filkins, K.6
-
2
-
-
0037339995
-
First-trimester nuchal translucency measurement and echocardiography at 16 to 18 weeks of gestation in prenatal detection for trisomy 18.
-
Cheng PJ, Liu CM, Chueh HY, Lin CM, Soong YK. First-trimester nuchal translucency measurement and echocardiography at 16 to 18 weeks of gestation in prenatal detection for trisomy 18. Prenat Diagn 2003;23:248-51.
-
(2003)
Prenat Diagn
, vol.23
, pp. 248-51
-
-
Cheng, P.J.1
Liu, C.M.2
Chueh, H.Y.3
Lin, C.M.4
Soong, Y.K.5
-
3
-
-
0034961816
-
Increased nuchal translucency, hydrops fetalis or hygroma colli: a new test strategy for early fetal aneuploidy detection.
-
Jenderny J, Schmidt W, Hecher K, Hackeloer BJ, Kerber S, Kochhan L, et al. Increased nuchal translucency, hydrops fetalis or hygroma colli: a new test strategy for early fetal aneuploidy detection. Fetal Diagn Ther 2001;16:211-4.
-
(2001)
Fetal Diagn Ther
, vol.16
, pp. 211-4
-
-
Jenderny, J.1
Schmidt, W.2
Hecher, K.3
Hackeloer, B.J.4
Kerber, S.5
Kochhan, L.6
-
4
-
-
0034041082
-
Screening for triploidy by fetal nuchal translucency and maternal serum free beta-hCG and PAPP-A at 10-14 weeks of gestation.
-
Spencer K, Liao AW, Skentou H, Cicero S, Nicolaides KH. Screening for triploidy by fetal nuchal translucency and maternal serum free beta-hCG and PAPP-A at 10-14 weeks of gestation. Prenat Diagn 2000;20:495-9.
-
(2000)
Prenat Diagn
, vol.20
, pp. 495-9
-
-
Spencer, K.1
Liao, A.W.2
Skentou, H.3
Cicero, S.4
Nicolaides, K.H.5
-
5
-
-
0037566040
-
Changes in nuchal translucency thickness in normal and abnormal karyotype fetuses.
-
Zoppi MA, Ibba RM, Floris M, Manca F, Axiana C, Monni G. Changes in nuchal translucency thickness in normal and abnormal karyotype fetuses. BJOG 2003;110:584-8.
-
(2003)
BJOG
, vol.110
, pp. 584-8
-
-
Zoppi, M.A.1
Ibba, R.M.2
Floris, M.3
Manca, F.4
Axiana, C.5
Monni, G.6
-
6
-
-
0033981975
-
Human male infertility: chromosome anomalies, meiotic disorders, abnormal spermatozoa and recurrent abortion.
-
Egozcue S, Blanco J, Vendrell JM, Garcia F, Veiga A, Aran B, et al. Human male infertility: chromosome anomalies, meiotic disorders, abnormal spermatozoa and recurrent abortion. Hum Reprod Update 2000;6:93-105.
-
(2000)
Hum Reprod Update
, vol.6
, pp. 93-105
-
-
Egozcue, S.1
Blanco, J.2
Vendrell, J.M.3
Garcia, F.4
Veiga, A.5
Aran, B.6
-
7
-
-
0041520974
-
Preimplantation genetic diagnosis of chromosome abnormalities: implications from the outcome for couples with chromosomal rearrangements.
-
Simopoulou M, Harper JC, Fragouli E, Mantzouratou A, Speyer BE, Serhal P, et al. Preimplantation genetic diagnosis of chromosome abnormalities: implications from the outcome for couples with chromosomal rearrangements. Prenat Diagn 2003;23:652-62.
-
(2003)
Prenat Diagn
, vol.23
, pp. 652-62
-
-
Simopoulou, M.1
Harper, J.C.2
Fragouli, E.3
Mantzouratou, A.4
Speyer, B.E.5
Serhal, P.6
-
8
-
-
0346725829
-
Preimplantation diagnosis of repeated miscarriage due to chromosomal translocations using metaphase chromosomes of a blastomere biopsied from 4- to 6-cell-stage embryos.
-
Tanaka A, Nagayoshi M, Awata S, Mawatari Y, Tanaka I, Kusunoki H. Preimplantation diagnosis of repeated miscarriage due to chromosomal translocations using metaphase chromosomes of a blastomere biopsied from 4- to 6-cell-stage embryos. Fertil Steril 2004;81:30-4.
-
(2004)
Fertil Steril
, vol.81
, pp. 30-4
-
-
Tanaka, A.1
Nagayoshi, M.2
Awata, S.3
Mawatari, Y.4
Tanaka, I.5
Kusunoki, H.6
-
9
-
-
4143052377
-
Patterns of chromosomal translocations identified by a birth defects registry, Hawaii, 1986-2000.
-
Forrester MB, Merz RD. Patterns of chromosomal translocations identified by a birth defects registry, Hawaii, 1986-2000. Genet Test 2004;8:204-8.
-
(2004)
Genet Test
, vol.8
, pp. 204-8
-
-
Forrester, M.B.1
Merz, R.D.2
-
10
-
-
1842683109
-
Chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) for a rapid first-trimester prenatal diagnosis.
-
Goumy C, Bonnet-Dupeyron MN, Cherasse Y, Laurichesse H, Jaffray JY, Lacroute G, et al. Chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) for a rapid first-trimester prenatal diagnosis. Prenat Diagn 2004;24:249-56.
-
(2004)
Prenat Diagn
, vol.24
, pp. 249-56
-
-
Goumy, C.1
Bonnet-Dupeyron, M.N.2
Cherasse, Y.3
Laurichesse, H.4
Jaffray, J.Y.5
Lacroute, G.6
-
11
-
-
0026562612
-
Fetal nuchal translucency: ultrasound screening for chromosomal defects in first trimester of pregnancy.
-
Nicolaides KH, Azar G, Byrne D, Mansur C, Marks K. Fetal nuchal translucency: ultrasound screening for chromosomal defects in first trimester of pregnancy. BMJ 1992;304:867-9.
-
(1992)
BMJ
, vol.304
, pp. 867-9
-
-
Nicolaides, K.H.1
Azar, G.2
Byrne, D.3
Mansur, C.4
Marks, K.5
-
13
-
-
0034817309
-
Nuchal translucency thickness and outcome in chromosome translocation diagnosed in the first trimester.
-
Sepulveda W, Be C, Youlton R, Carstens E, Reyes M. Nuchal translucency thickness and outcome in chromosome translocation diagnosed in the first trimester. Prenat Diagn 2001;21:726-8.
-
(2001)
Prenat Diagn
, vol.21
, pp. 726-8
-
-
Sepulveda, W.1
Be, C.2
Youlton, R.3
Carstens, E.4
Reyes, M.5
-
14
-
-
0037957045
-
Pathophysiology of increased nuchal translucency: a review of the literature.
-
Haak MC, van Vugt JM. Pathophysiology of increased nuchal translucency: a review of the literature. Hum Reprod Update 2003;9:175-84.
-
(2003)
Hum Reprod Update
, vol.9
, pp. 175-84
-
-
Haak, M.C.1
van Vugt, J.M.2
-
15
-
-
0028863134
-
Increased nuchal translucency in trisomy 21 fetuses: relationship to narrowing of the aortic isthmus.
-
Hyett J, Moscoso G, Nicolaides K. Increased nuchal translucency in trisomy 21 fetuses: relationship to narrowing of the aortic isthmus. Hum Reprod 1995;10:3049-51.
-
(1995)
Hum Reprod
, vol.10
, pp. 3049-51
-
-
Hyett, J.1
Moscoso, G.2
Nicolaides, K.3
-
16
-
-
0031047257
-
Abnormalities of the heart and great arteries in first trimester chromosomally abnormal fetuses.
-
Hyett J, Moscoso G, Nicolaides K. Abnormalities of the heart and great arteries in first trimester chromosomally abnormal fetuses. Am J Med Genet 1997;69:207-16.
-
(1997)
Am J Med Genet
, vol.69
, pp. 207-16
-
-
Hyett, J.1
Moscoso, G.2
Nicolaides, K.3
-
17
-
-
0038340988
-
Disease associated balanced chromosome rearrangements (DBCR): report of two new cases.
-
Tonk VS, Wyandt HE, Huang X, Patel N, Morgan DL, Kukolich M, et al. Disease associated balanced chromosome rearrangements (DBCR): report of two new cases. Ann Genet 2003;46:37-43.
-
(2003)
Ann Genet
, vol.46
, pp. 37-43
-
-
Tonk, V.S.1
Wyandt, H.E.2
Huang, X.3
Patel, N.4
Morgan, D.L.5
Kukolich, M.6
-
18
-
-
0020521245
-
Balanced translocations among couples with two or more spontaneous abortions: are males and females equally likely to be carriers?
-
Lippman-Hand A, Vekemans M. Balanced translocations among couples with two or more spontaneous abortions: are males and females equally likely to be carriers? Hum Genet 1983;63:252-7.
-
(1983)
Hum Genet
, vol.63
, pp. 252-7
-
-
Lippman-Hand, A.1
Vekemans, M.2
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