-
1
-
-
0033157098
-
Utility of M-Fish in clinical cytogenetics
-
Ialal SM, Law, ME. Utility of M-Fish in clinical cytogenetics. Genetics in Medicine 1999;1:181-186.
-
(1999)
Genetics in Medicine
, vol.1
, pp. 181-186
-
-
Ialal, S.M.1
Law, M.E.2
-
2
-
-
0032195407
-
Clinical applications of comparative genomic hybridization
-
Lew B, Dunn TM, Kaffe S, Kardon N, Hirschorn K. Clinical applications of comparative genomic hybridization. Genetics in Medicine 1998;1:4-12.
-
(1998)
Genetics in Medicine
, vol.1
, pp. 4-12
-
-
Lew, B.1
Dunn, T.M.2
Kaffe, S.3
Kardon, N.4
Hirschorn, K.5
-
3
-
-
0343319476
-
Fluorescence in situ hybridization with human chromosome specific libraries: Detection of trisomv 21 and translocation of chromosome 4
-
Pinkel D, Landegent I, Collins C, Fuscoe I, Segraves R, Lucas I, Gray JW. Fluorescence in situ hybridization with human chromosome specific libraries: Detection of trisomv 21 and translocation of chromosome 4. Proc Natl Acad Sei USA 1988;85:9138-9142.
-
(1988)
Proc Natl Acad Sei USA
, vol.85
, pp. 9138-9142
-
-
Pinkel, D.1
Landegent, I.2
Collins, C.3
Fuscoe, I.4
Segraves, R.5
Lucas, I.6
Gray, J.W.7
-
4
-
-
0023691590
-
Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome specific library probes
-
Cremer T, Lichter P, Borden I, Ward DC, Manuelidis L. Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome specific library probes. Hum Genet 1988;80:235-246.
-
(1988)
Hum Genet
, vol.80
, pp. 235-246
-
-
Cremer, T.1
Lichter, P.2
Borden, I.3
Ward, D.C.4
Manuelidis, L.5
-
5
-
-
0023692635
-
Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using chromosome specific library probes
-
Lichter P, Cremer T, Borden I, Manuelidis L, Ward DC. Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using chromosome specific library probes. Hum Genet 1988;80:224-234.
-
(1988)
Hum Genet
, vol.80
, pp. 224-234
-
-
Lichter, P.1
Cremer, T.2
Borden, I.3
Manuelidis, L.4
Ward, D.C.5
-
6
-
-
0031769001
-
Identification of de novo chromosomal markers and derivatives by spectral karyotyping
-
Haddad BR, Schrock E, Meck I, Cowan J, Young H, Ferguson-Smith MA, du Manoir S, Ried T. Identification of de novo chromosomal markers and derivatives by spectral karyotyping. Hum Genet 1998;103:619-625.
-
(1998)
Hum Genet
, vol.103
, pp. 619-625
-
-
Haddad, B.R.1
Schrock, E.2
Meck, I.3
Cowan, J.4
Young, H.5
Ferguson-Smith, M.A.6
Du Manoir, S.7
Ried, T.8
-
7
-
-
0031772122
-
Identification of an unusual marker chromosome by spectral karyotyping
-
Huang B, Ning V, Lamb AN, Sandlin CL, lamehdor M, Ried T, Bartley I. Identification of an unusual marker chromosome by spectral karyotyping. Am/Med Genet 1998;80:368-372.
-
(1998)
Am/Med Genet
, vol.80
, pp. 368-372
-
-
Huang, B.1
Ning, V.2
Lamb, A.N.3
Sandlin, C.L.4
Lamehdor, M.5
Ried, T.6
Bartley, I.7
-
8
-
-
0031729663
-
FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16
-
Phelan MC, Blackburn W, Rogers RC, Crawford EC, Cooley NRI, Schröck E, Ning Y, Ried T. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16. Prenat Diagn 1998; 18:1174-1180.
-
(1998)
Prenat Diagn
, vol.18
, pp. 1174-1180
-
-
Phelan, M.C.1
Blackburn, W.2
Rogers, R.C.3
Crawford, E.C.4
Cooley, N.5
Schröck, E.6
Ning, Y.7
Ried, T.8
-
9
-
-
2642683176
-
Spectral karvotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities
-
Schröck E, Veldman T, Padilla-Nash H, Ning Y, Spurbeck I, Jalal S, Shaffer LG, Papenhausen P, Kozma C, Phelan MC, Kjeldsen E, Schonberg SA, O'Brien P, Biesecker L, du Manoir S, Ried T. Spectral karvotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities. Hum Genet 1997;101:255-262.
-
(1997)
Hum Genet
, vol.101
, pp. 255-262
-
-
Schröck, E.1
Veldman, T.2
Padilla-Nash, H.3
Ning, Y.4
Spurbeck, I.5
Jalal, S.6
Shaffer, L.G.7
Papenhausen, P.8
Kozma, C.9
Phelan, M.C.10
Kjeldsen, E.11
Schonberg, S.A.12
O'brien, P.13
Biesecker, L.14
Du Manoir, S.15
Ried, T.16
-
10
-
-
0032477707
-
FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15. 11. Review of Literature
-
Crolla IA. FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15. 11. Review of Literature. Am I Med Genet 1998;75:367-381.
-
(1998)
Am I Med Genet
, vol.75
, pp. 367-381
-
-
Crolla, I.A.1
-
11
-
-
0032477780
-
FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15 and 22.1. Results of 26 new cases
-
Crolla IA, Long F, Rivera H, Dennis NR. FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15 and 22.1. Results of 26 new cases. Am I Med Genet 1998;75:355-366.
-
(1998)
Am I Med Genet
, vol.75
, pp. 355-366
-
-
Crolla, I.A.1
Long, F.2
Rivera, H.3
Dennis, N.R.4
-
12
-
-
0031007675
-
Sex chromosome markers: Characterization using fluorescence in situ hybridization and review of literature
-
Schwartz S, Depinet TW, Leana-Cox L, Isada NB, Karson EM, Park VM, Pasztor LM, Sheppard LC, Stallard R, Wolff DJ, Zinn AB, Zürcher VL, Zackowski L. Sex chromosome markers: Characterization using fluorescence in situ hybridization and review of literature. Am J Med Genet 1997;71:1-7.
-
(1997)
Am J Med Genet
, vol.71
, pp. 1-7
-
-
Schwartz, S.1
Depinet, T.W.2
Leana-Cox, L.3
Isada, N.B.4
Karson, E.M.5
Park, V.M.6
Pasztor, L.M.7
Sheppard, L.C.8
Stallard, R.9
Wolff, D.J.10
Zinn, A.B.11
Zürcher, V.L.12
Zackowski, L.13
-
14
-
-
0028205957
-
Molecular cytogenetic analysis of inv dup (151 chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: Clinical implications
-
Lena-Cox I, lenkins L, Palmer CG, Plattner R, Sheppard L, Flejter WL, Zackowski I, Tsien F, Schwartz S. Molecular cytogenetic analysis of inv dup 151 chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: Clinical implications. Am/Hum Genet 1994;54:748-756.
-
(1994)
Am/Hum Genet
, vol.54
, pp. 748-756
-
-
Lena-Cox, I.1
Lenkins, L.2
Palmer, C.G.3
Plattner, R.4
Sheppard, L.5
Flejter, W.L.6
Zackowski, I.7
Tsien, F.8
Schwartz, S.9
-
15
-
-
0027365064
-
Characterization of de novo duplications in eight patients by using fluorescence in situ hybridization with chromosome-specific DNA libraries
-
Lena-Cox J, Levin S, Surana R, Wulfsberg E, Keene CL, Raftel LI, Sullivan B, Schwartz S. Characterization of de novo duplications in eight patients by using fluorescence in situ hybridization with chromosome-specific DNA libraries. Am/Hum Genet 1993;52:1067-1073.
-
(1993)
Am/Hum Genet
, vol.52
, pp. 1067-1073
-
-
Lena-Cox, J.1
Levin, S.2
Surana, R.3
Wulfsberg, E.4
Keene, C.L.5
Raftel, L.I.6
Sullivan, B.7
Schwartz, S.8
-
16
-
-
0031714587
-
Molecular characterization and delineation of subtle deletions in de novo “balanced” chromosomal rearrangements
-
Kumar A, Becker LA, Depinet TW, Haren M, Kurtz CL, Robin NH, Cassidy SB, Wolff DI, Schwartz S. Molecular characterization and delineation of subtle deletions in de novo “balanced” chromosomal rearrangements. Hum Genet 1998; 103:173-178.
-
(1998)
Hum Genet
, vol.103
, pp. 173-178
-
-
Kumar, A.1
Becker, L.A.2
Depinet, T.W.3
Haren, M.4
Kurtz, C.L.5
Robin, N.H.6
Cassidy, S.B.7
Wolff, D.I.8
Schwartz, S.9
-
17
-
-
0033188174
-
Molecular refinement of karyo type: Beyond the cytogenetic band
-
press
-
Sirko-Osadsa A, Cassidy SB, Depinet TW, Robin NH, Limwongse C, Schwartz S. Molecular refinement of karyo type: Beyond the cytogenetic band. Genetics in Medicine 1999;6: In press.
-
(1999)
Genetics in Medicine
, pp. 6
-
-
Sirko-Osadsa, A.1
Cassidy, S.B.2
Depinet, T.W.3
Robin, N.H.4
Limwongse, C.5
Schwartz, S.6
-
19
-
-
0030960829
-
Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres
-
Knight S, Horsley SW, Regan R, Lawrie NM, Maher EJ, Cardy DL, Flint I, Kearney L. Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres. Eur/Hum Genet 1997;5:1-8.
-
(1997)
Eur/Hum Genet
, vol.5
, pp. 1-8
-
-
Knight, S.1
Horsley, S.W.2
Regan, R.3
Lawrie, N.M.4
Maher, E.J.5
Cardy, D.L.6
Flint, I.7
Kearney, L.8
-
20
-
-
0028798545
-
The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
-
Flint I, Wilkie AO, Buckle VI, Winter RM, Holland A, McDermid HE. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation. Nat Genet 1995;9:132-140.
-
(1995)
Nat Genet
, vol.9
, pp. 132-140
-
-
Flint, I.1
Wilkie, A.O.2
Buckle, V.I.3
Winter, R.M.4
Holland, A.5
Mc Dermid, H.E.6
-
21
-
-
0027365371
-
Rapid prenatal diagnosis of chromosomal aneuploi-dies by fluorescence in situ hybridization: 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 aneuploi-dies by fluorescence in situ hybridization: Clinical experience with 4500 specimens. Am Hum Genet 1993;52:854-865.
-
(1993)
Am Hum Genet
, vol.52
, pp. 854-865
-
-
Ward, B.E.1
Gersen, S.L.2
Carelli, M.P.3
Mc Guire, N.M.4
Dackowski, W.R.5
Weinstein, M.6
Sandlin, C.7
Warren, R.8
Klinger, K.W.9
-
22
-
-
0032079490
-
Highly sensitive fluorescence in situ hybridization method to detect double BCR/ABL fusion and monitor response to therapy in chronic myeloid leukemia
-
Deward GW, Wyatt WA, Juneau AL, Carlson RO, Zinsmeister AR, Jalal SM, Spurbeck IL, Silver RT. Highly sensitive fluorescence in situ hybridization method to detect double BCR/ABL fusion and monitor response to therapy in chronic myeloid leukemia. Blood 1998;91:3357-3365.
-
(1998)
Blood
, vol.91
, pp. 3357-3365
-
-
Deward, G.W.1
Wyatt, W.A.2
Juneau, A.L.3
Carlson, R.O.4
Zinsmeister, A.R.5
Jalal, S.M.6
Spurbeck, I.L.7
Silver, R.T.8
-
23
-
-
0029912473
-
Karyotyping human chromosomes by combinatorial multi-fluor FISH
-
Speicher MR, Ballard SG, Ward DC. Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nat Genet 1996;12:368-375.
-
(1996)
Nat Genet
, vol.12
, pp. 368-375
-
-
Speicher, M.R.1
Ballard, S.G.2
Ward, D.C.3
-
24
-
-
0038214755
-
Multicolor spectral karyotyping of human chromosomes
-
Schröck E, du Manoir S, Veldman T, Schoell B, Wienberg I, Ferguson-Smith MA, Ning Y, Ledbetter DH, Bar-Am I, Soenksen D, Garini Y, Ried T. Multicolor spectral karyotyping of human chromosomes. Science 1996;273:494-497.
-
(1996)
Science
, vol.273
, pp. 494-497
-
-
Schröck, E.1
Du Manoir, S.2
Veldman, T.3
Schoell, B.4
Wienberg, I.5
Ferguson-Smith, M.A.6
Ning, Y.7
Ledbetter, D.H.8
Bar-Am, I.9
Soenksen, D.10
Garini, Y.11
Ried, T.12
-
25
-
-
0037550237
-
A novel source of highly specific chromosome painting probes for human karyotype analysis derived from primate homologues
-
Muller S, O'Brien PC, Ferguson-Smith MA, Wienberg I. A novel source of highly specific chromosome painting probes for human karyotype analysis derived from primate homologues. Hum Genet 1997;101:149-153.
-
(1997)
Hum Genet
, vol.101
, pp. 149-153
-
-
Muller, S.1
O'brien, P.C.2
Ferguson-Smith, M.A.3
Wienberg, I.4
-
26
-
-
0032403372
-
Cross-species colour segmenting: A novel tool in human karyotype analysis
-
Muller S, O’Brien PC, Ferguson-Smith MA, Wienberg I. Cross-species colour segmenting: A novel tool in human karyotype analysis. Cytometry 1998;33: 445-452.
-
(1998)
Cytometry
, vol.33
, pp. 445-452
-
-
Muller, S.1
O’Brien, P.C.2
Ferguson-Smith, M.A.3
Wienberg, I.4
-
27
-
-
0345293892
-
Toward a multicolor chromosome bar code for the entire human karyotype by fluorescence in situ hybridization
-
Muller S, Rocchi M, Ferguson-Smith MA, Wienberg J. Toward a multicolor chromosome bar code for the entire human karyotype by fluorescence in situ hybridization. Hum Genet 1997;100:271-278.
-
(1997)
Hum Genet
, vol.100
, pp. 271-278
-
-
Muller, S.1
Rocchi, M.2
Ferguson-Smith, M.A.3
Wienberg, J.4
-
28
-
-
0033053010
-
High resolution multicolor-banding: A new technique for refined FISH analysis of human chromosomes
-
Chudoba I, Plesch A, Lorch T, Lemke I, Claussen U, Senger G. High resolution multicolor-banding: A new technique for refined FISH analysis of human chromosomes. Cytogenet Cell Genet 1999;84:156-160.
-
(1999)
Cytogenet Cell Genet
, vol.84
, pp. 156-160
-
-
Chudoba, I.1
Plesch, A.2
Lorch, T.3
Lemke, I.4
Claussen, U.5
Senger, G.6
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