-
1
-
-
0026582134
-
Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridisation
-
Christensen B, Bryndorf T, Philip J, Lundsteen C, Hansen W. Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridisation. Prenat Diagn 1992: 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
-
2
-
-
0026738541
-
Continuum of overlapping clones spanning the entire human chromosome 21q
-
Chumakov I, Rigault P, Giullou S, Ougen P, Billaut A, Guasconi G, Gervy P, LeGall I, et al. Continuum of overlapping clones spanning the entire human chromosome 21q. Nature 1993: 359: 380-387.
-
(1993)
Nature
, vol.359
, pp. 380-387
-
-
Chumakov, I.1
Rigault, P.2
Giullou, S.3
Ougen, P.4
Billaut, A.5
Guasconi, G.6
Gervy, P.7
LeGall, I.8
-
3
-
-
0027793704
-
Mapping the Down syndrome chromosome region. Establishment of a YAC contig spanning 1.2 megabases
-
Crete N, Gosset PH, Theophile D, Duterque-Coquillaud M, Blouin J-L, Vayessettes C, Sinet PM, Creau-Goldberg N. Mapping the Down syndrome chromosome region. Establishment of a YAC contig spanning 1.2 megabases. Eur J Hum Genet 1993: 1: 51-63.
-
(1993)
Eur J Hum Genet
, vol.1
, pp. 51-63
-
-
Crete, N.1
Gosset, P.H.2
Theophile, D.3
Duterque-Coquillaud, M.4
Blouin, J.-L.5
Vayessettes, C.6
Sinet, P.M.7
Creau-Goldberg, N.8
-
4
-
-
0001038798
-
Human chromosome specific partial digest libraries in lambda and cosmid vectors
-
deJong PJ, Yokobata K, Chen C, Lohman F, Pederson L, McNinch J, van Dilla M. Human chromosome specific partial digest libraries in lambda and cosmid vectors. Cytogenet Cell Genet 1989: 51: 985.
-
(1989)
Cytogenet Cell Genet
, vol.51
, pp. 985
-
-
DeJong, P.J.1
Yokobata, K.2
Chen, C.3
Lohman, F.4
Pederson, L.5
McNinch, J.6
Van Dilla, M.7
-
5
-
-
0022967803
-
Construction of human chromosome specific DNA libraries from flow sorted human chromosomes
-
Deaven LL, van Dilla MA, Bartholdi MF, Carrano AV, Cram RS, Fuscie JC, Gray JW, Hildebrand CE, Moyzis RK, Perlman J. Construction of human chromosome specific DNA libraries from flow sorted human chromosomes. Cold Spring Harbor Symp Quant Biol 1986: 51: 159-168.
-
(1986)
Cold Spring Harbor Symp Quant Biol
, vol.51
, pp. 159-168
-
-
Deaven, L.L.1
Van Dilla, M.A.2
Bartholdi, M.F.3
Carrano, A.V.4
Cram, R.S.5
Fuscie, J.C.6
Gray, J.W.7
Hildebrand, C.E.8
Moyzis, R.K.9
Perlman, J.10
-
6
-
-
0027874350
-
Molecular mapping of twenty-four features of Down syndrome on chromosome 21
-
Delabar J-M, Theophile D, Rahmani Z, Chettouh Z, Blouin J-L, Prieur M, Noel B, Sinet PM. Molecular mapping of twenty-four features of Down syndrome on chromosome 21. Eur J Hum Genet 1993: 1: 114-124.
-
(1993)
Eur J Hum Genet
, vol.1
, pp. 114-124
-
-
Delabar, J.-M.1
Theophile, D.2
Rahmani, Z.3
Chettouh, Z.4
Blouin, J.-L.5
Prieur, M.6
Noel, B.7
Sinet, P.M.8
-
7
-
-
0028344760
-
3.6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21
-
Dufresne-Zacharia MC, Dahmane N, Theophile D, Orti R, Chettouh Z, Sinet PM, Delabar JM. 3.6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21. Genomics 1994: 19: 462-469.
-
(1994)
Genomics
, vol.19
, pp. 462-469
-
-
Dufresne-Zacharia, M.C.1
Dahmane, N.2
Theophile, D.3
Orti, R.4
Chettouh, Z.5
Sinet, P.M.6
Delabar, J.M.7
-
8
-
-
0026636703
-
Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridisation (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. Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridisation (FISH). Am J Hum Genet 1992: 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
-
10
-
-
0025881002
-
Detection of aneuploidy involving chromosome 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes
-
Kuo WL, Tenjin H, Segraves R, Pinkel D, Golbus MS, Gray J. Detection of aneuploidy involving chromosome 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes. Am J Hum Genet 1991: 49: 112-119.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 112-119
-
-
Kuo, W.L.1
Tenjin, H.2
Segraves, R.3
Pinkel, D.4
Golbus, M.S.5
Gray, J.6
-
11
-
-
0027214602
-
Integration of gene maps: Chromosome 21
-
Lawrence S, Collins A, Keats BJ, Hulten M, Morton NE. Integration of gene maps: chromosome 21. PNAS 1993: 90: 7210-7214.
-
(1993)
PNAS
, vol.90
, pp. 7210-7214
-
-
Lawrence, S.1
Collins, A.2
Keats, B.J.3
Hulten, M.4
Morton, N.E.5
-
12
-
-
0026693187
-
Prenatal diagnosis with repetitive in situ hybridisation probes
-
Lebo RV, Flandrmeyer RR, Diukman R, Lynch ED, Lepercq JA, Golbus MS. Prenatal diagnosis with repetitive in situ hybridisation probes. Am J Med Genet 1992: 43: 848-854.
-
(1992)
Am J Med Genet
, vol.43
, pp. 848-854
-
-
Lebo, R.V.1
Flandrmeyer, R.R.2
Diukman, R.3
Lynch, E.D.4
Lepercq, J.A.5
Golbus, M.S.6
-
13
-
-
0000579784
-
Chromosome analysis by non-isotopic in situ hybridisation
-
Rooney DE, Czepulkowski BH, eds. IRL Press
-
Lichter P, Cremer T. Chromosome analysis by non-isotopic in situ hybridisation. In: Rooney DE, Czepulkowski BH, eds. Human cytogenetics - a practical approach. IRL Press, 1992.
-
(1992)
Human Cytogenetics - A Practical Approach
-
-
Lichter, P.1
Cremer, T.2
-
14
-
-
0024712933
-
Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21
-
McCormick MK, Schinzel A, Petersen MB, Stetten G, Driscoll DJ, Cantu ES, Tranebjaerg L, Mikkelsen M, Watkins PC, Antonarakis SE. Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21. Genomics 1989: 5: 325-331.
-
(1989)
Genomics
, vol.5
, pp. 325-331
-
-
McCormick, M.K.1
Schinzel, A.2
Petersen, M.B.3
Stetten, G.4
Driscoll, D.J.5
Cantu, E.S.6
Tranebjaerg, L.7
Mikkelsen, M.8
Watkins, P.C.9
Antonarakis, S.E.10
-
15
-
-
0026345290
-
Construction arraying and high density screening of large insert libraries of the human chromosomes X and 21: Their potential use of reference libraries
-
Nizetic D, Zehetner G, Monaco AP, Gellen L, Young BD, Lehrach H. Construction arraying and high density screening of large insert libraries of the human chromosomes X and 21: their potential use of reference libraries. PNAS 1991: 88: 3233-3237.
-
(1991)
PNAS
, vol.88
, pp. 3233-3237
-
-
Nizetic, D.1
Zehetner, G.2
Monaco, A.P.3
Gellen, L.4
Young, B.D.5
Lehrach, H.6
-
16
-
-
0028231476
-
An integrated YAC overlap and "cosmid-pocket" map of the human chromosome 21
-
Nizetic D, Gellen L, Hamvas R, Mott R, Grigoriev A, Vatcheva R, Zehetner G, Yaspo ML, Dutriax A, Lopes C, Delabar JM, Van Broeckhoven C, Potier MC, Lehrach H. An integrated YAC overlap and "cosmid-pocket" map of the human chromosome 21. Hum Molec Genet 1994a: 3: 759-770.
-
(1994)
Hum Molec Genet
, vol.3
, pp. 759-770
-
-
Nizetic, D.1
Gellen, L.2
Hamvas, R.3
Mott, R.4
Grigoriev, A.5
Vatcheva, R.6
Zehetner, G.7
Yaspo, M.L.8
Dutriax, A.9
Lopes, C.10
Delabar, J.M.11
Van Broeckhoven, C.12
Potier, M.C.13
Lehrach, H.14
-
17
-
-
0028675056
-
Construction of cosmid libraries from flow sorted human chromosomes 1, 6, 7, 11, 13, 18 for reference library resources
-
Nizetic D, Monard S, Young BD, Cotter F, Zehetner G, Lehrach H. Construction of cosmid libraries from flow sorted human chromosomes 1, 6, 7, 11, 13, 18 for reference library resources. Mammalian Genome 1994b: 5: 801-802.
-
(1994)
Mammalian Genome
, vol.5
, pp. 801-802
-
-
Nizetic, D.1
Monard, S.2
Young, B.D.3
Cotter, F.4
Zehetner, G.5
Lehrach, H.6
-
18
-
-
0028076769
-
High resolution physical map of the 2.5 Mbp of the Down syndrome region on chromosome 21
-
Patil N, Peterson A, Rothman A, deJong PJ, Myers RM, Cox DR. High resolution physical map of the 2.5 Mbp of the Down syndrome region on chromosome 21. Hum Mol Genet 1994: 3: 1811-1817.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1811-1817
-
-
Patil, N.1
Peterson, A.2
Rothman, A.3
DeJong, P.J.4
Myers, R.M.5
Cox, D.R.6
-
19
-
-
0012083187
-
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome
-
Rahmani Z, Blouin JL, Creau-Goldberg N, Watkins PC, Mattei JF, Poissonier M, Prieur M, et al. Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome. PNAS 1989: 86: 5958-5962.
-
(1989)
PNAS
, vol.86
, pp. 5958-5962
-
-
Rahmani, Z.1
Blouin, J.L.2
Creau-Goldberg, N.3
Watkins, P.C.4
Mattei, J.F.5
Poissonier, M.6
Prieur, M.7
-
20
-
-
0027712163
-
Molecular mapping of the Down syndrome phenotype on chromosome 21
-
Epstein CJ, ed. Wiley-Liss Inc.
-
Sinet PM, Theophile D, Rahmani Z, Chettouh Z, Blouin JL, Prieur M, Nole B, Delabar JM. Molecular mapping of the Down syndrome phenotype on chromosome 21. In: Epstein CJ, ed. The phenotypic mapping of Down syndrome and other aneuploid conditions. Wiley-Liss Inc., 1993: 63-86.
-
(1993)
The Phenotypic Mapping of Down Syndrome and Other Aneuploid Conditions
, pp. 63-86
-
-
Sinet, P.M.1
Theophile, D.2
Rahmani, Z.3
Chettouh, Z.4
Blouin, J.L.5
Prieur, M.6
Nole, B.7
Delabar, J.M.8
-
21
-
-
0027365371
-
Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridisation: Clinical experience with 4500 specimens
-
Ward BE, Gersen SL, Carelli MP, McGuire NM, Dackowski WR, Weinstein M, Sandlin C, Warren R, Klinger KW. Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridisation: 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
McGuire, N.M.4
Dackowski, W.R.5
Weinstein, M.6
Sandlin, C.7
Warren, R.8
Klinger, K.W.9
-
22
-
-
0026458166
-
Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridisation using a cosmid contig
-
Zheng YL, Ferguson-Smith MA, Warner JP, Ferguson-Smith ME, Sargent CA, Carter NP. Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridisation using a cosmid contig. Prenat Diagn 1992: 12: 931-943.
-
(1992)
Prenat Diagn
, vol.12
, pp. 931-943
-
-
Zheng, Y.L.1
Ferguson-Smith, M.A.2
Warner, J.P.3
Ferguson-Smith, M.E.4
Sargent, C.A.5
Carter, N.P.6
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