-
1
-
-
0028198442
-
Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization
-
Cacheux, V., Tachdjian, G., Druart, L., Oury, J.F., Sérero, S., Blot, P., Nessmann, C. (1994). Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization, Prenat. Diagn., 14, 79-86.
-
(1994)
Prenat. Diagn.
, vol.14
, pp. 79-86
-
-
Cacheux, V.1
Tachdjian, G.2
Druart, L.3
Oury, J.F.4
Sérero, S.5
Blot, P.6
Nessmann, C.7
-
2
-
-
0026582134
-
Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridization
-
Christensen, B., Bryndorf, T., Philip, J., Lundsteen, C., Hansen, W. (1992). Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridization, Prenat. Diagn., 12, 241-250.
-
(1992)
Prenat. Diagn.
, vol.12
, pp. 241-250
-
-
Christensen, B.1
Bryndorf, T.2
Philip, J.3
Lundsteen, C.4
Hansen, W.5
-
3
-
-
0029824227
-
Early prenatal diagnosis: Standard cytogenetic analysis of coelomic cells obtained by coelocentesis
-
Crüger, D.G., Bruun-Petersen, G., Kølvraa, S. (1997). Early prenatal diagnosis: standard cytogenetic analysis of coelomic cells obtained by coelocentesis, Prenat. Diagn., 16, 945-949.
-
(1997)
Prenat. Diagn.
, vol.16
, pp. 945-949
-
-
Crüger, D.G.1
Bruun-Petersen, G.2
Kølvraa, S.3
-
5
-
-
1842297190
-
Chromosome specificity of human repetitive DNA
-
Devilee, P., Cremer, T., Bakker, E., Wapenaar, M.C., Kievits, T., Slieker, W.A.T., Slagboom, P.E., Scholl, H.P., Hager, H.D., Stevenson, A.G.F., Pearson, P.L. (1985). Chromosome specificity of human repetitive DNA, Cytogenet. Cell Genet., 40, 616.
-
(1985)
Cytogenet. Cell Genet.
, vol.40
, pp. 616
-
-
Devilee, P.1
Cremer, T.2
Bakker, E.3
Wapenaar, M.C.4
Kievits, T.5
Slieker, W.A.T.6
Slagboom, P.E.7
Scholl, H.P.8
Hager, H.D.9
Stevenson, A.G.F.10
Pearson, P.L.11
-
6
-
-
0022587147
-
Two subsets of human alphoid repetitive DNA show distinct preferential location in the pericentric regions of chromosomes 13, 18 and 21
-
Devilee, P., Cremer, T., Slagboom, P.E., Bakker, E., Scholl, H.P., Hager, H.D., Stevenson, A.G.F., Cornelissee, C.J., Pearson, P.L. (1986). Two subsets of human alphoid repetitive DNA show distinct preferential location in the pericentric regions of chromosomes 13, 18 and 21, Cytogenet. Cell Genet., 41, 193-201.
-
(1986)
Cytogenet. Cell Genet.
, vol.41
, pp. 193-201
-
-
Devilee, P.1
Cremer, T.2
Slagboom, P.E.3
Bakker, E.4
Scholl, H.P.5
Hager, H.D.6
Stevenson, A.G.F.7
Cornelissee, C.J.8
Pearson, P.L.9
-
7
-
-
0027204961
-
Coelocentesis: A new technique for early prenatal diagnosis
-
Jurkovic, D., Jauniaux, E., Campbell, S., Pandya, P., Cardy, D.L., Nicolaides, K.H. (1993). Coelocentesis: a new technique for early prenatal diagnosis, Lancet, 341, 1623-1624.
-
(1993)
Lancet
, vol.341
, pp. 1623-1624
-
-
Jurkovic, D.1
Jauniaux, E.2
Campbell, S.3
Pandya, P.4
Cardy, D.L.5
Nicolaides, K.H.6
-
8
-
-
0026636703
-
Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH)
-
Klinger, K., Landes, G., Shook, D., Harvey, R., Lopez, L., Locke, P., Lerner, T., Osathanondh, R., Leverone, B., Houseal, T., Pavelka, K., Dackowski, W. (1992). Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH), Am. J. Hum. Genet., 51, 55-65.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 55-65
-
-
Klinger, K.1
Landes, G.2
Shook, D.3
Harvey, R.4
Lopez, L.5
Locke, P.6
Lerner, T.7
Osathanondh, R.8
Leverone, B.9
Houseal, T.10
Pavelka, K.11
Dackowski, W.12
-
9
-
-
0025881002
-
Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes
-
Kou, W.L., Tenjin, H., Segraves, R., Pinkel, D., Golbus, M.S., Gray, J. (1991). Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes, Am. J. Hum. Genet., 49, 112-119.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 112-119
-
-
Kou, W.L.1
Tenjin, H.2
Segraves, R.3
Pinkel, D.4
Golbus, M.S.5
Gray, J.6
-
10
-
-
0026693187
-
Prenatal diagnosis with repetitive in situ hybridization probes
-
Lebo, R.V., Flandermeyer, R.R., Diukman, R., Lynch, E.D., Lepercq, J.A., Golbus, M.S. (1992). Prenatal diagnosis with repetitive in situ hybridization probes, Am. J. Hum. Genet., 43, 848-854.
-
(1992)
Am. J. Hum. Genet.
, vol.43
, pp. 848-854
-
-
Lebo, R.V.1
Flandermeyer, R.R.2
Diukman, R.3
Lynch, E.D.4
Lepercq, J.A.5
Golbus, M.S.6
-
11
-
-
0028676251
-
Prenatal aneuploidy detection in interphase cells by fluorescence in situ hybridization (FISH)
-
Philip, J., Bryndorf, T., Christensen, B. (1994). Prenatal aneuploidy detection in interphase cells by fluorescence in situ hybridization (FISH), Prenat. Diagn., 14, 1203-1215.
-
(1994)
Prenat. Diagn.
, vol.14
, pp. 1203-1215
-
-
Philip, J.1
Bryndorf, T.2
Christensen, B.3
-
12
-
-
0028149132
-
Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: A prospective study
-
Spathas, D.H., Divane, A., Maniatis, G.M., Ferguson-Smith, M.E., Ferguson-Smith, M.A. (1994). Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: a prospective study, Prenat. Diagn., 14, 1049-1054.
-
(1994)
Prenat. Diagn.
, vol.14
, pp. 1049-1054
-
-
Spathas, D.H.1
Divane, A.2
Maniatis, G.M.3
Ferguson-Smith, M.E.4
Ferguson-Smith, M.A.5
-
13
-
-
0021100775
-
Isolation and characterization of a major tandem repeat family from the human X chromosome
-
Willard, H.F., Smith, K.D., Sutherland, J. (1983). Isolation and characterization of a major tandem repeat family from the human X chromosome, Nucleic Acids Res., 11, 2017-2033.
-
(1983)
Nucleic Acids Res.
, vol.11
, pp. 2017-2033
-
-
Willard, H.F.1
Smith, K.D.2
Sutherland, J.3
-
14
-
-
0022401559
-
Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome
-
Wolfe, J., Darling, S.M., Erickson, R.P., Craig, I.W., Buckle, V.J., Rigby, P.W.J., Willard, H.F., Goodfellow, P.N. (1985). Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome, J. Mol. Biol., 182, 477-485.
-
(1985)
J. Mol. Biol.
, vol.182
, pp. 477-485
-
-
Wolfe, J.1
Darling, S.M.2
Erickson, R.P.3
Craig, I.W.4
Buckle, V.J.5
Rigby, P.W.J.6
Willard, H.F.7
Goodfellow, P.N.8
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