-
1
-
-
0016348695
-
Distinct hematological disorder with deletion of long arm of no. 5 chromosome
-
Van den Berghe H, Cassiman JJ, David G, Fryns JP, Michaux JL, Sokal G: Distinct hematological disorder with deletion of long arm of no. 5 chromosome. Nature 251:437, 1974
-
(1974)
Nature
, vol.251
, pp. 437
-
-
Van Den Berghe, H.1
Cassiman, J.J.2
David, G.3
Fryns, J.P.4
Michaux, J.L.5
Sokal, G.6
-
2
-
-
0023607867
-
The 5q- abnormality
-
Nimer SD, Golde DW: The 5q- abnormality. Blood 70:1705, 1987
-
(1987)
Blood
, vol.70
, pp. 1705
-
-
Nimer, S.D.1
Golde, D.W.2
-
3
-
-
0020586056
-
Morphologic and cytochemical observations on the overt leukemia phase of therapy-related leukemia
-
Vardiman JW, Coelho A, Golomb HM, Rowley J: Morphologic and cytochemical observations on the overt leukemia phase of therapy-related leukemia. Am J Clin Pathol 79:525, 1983
-
(1983)
Am J Clin Pathol
, vol.79
, pp. 525
-
-
Vardiman, J.W.1
Coelho, A.2
Golomb, H.M.3
Rowley, J.4
-
4
-
-
0025046596
-
Chromosome aberrations and prognostic factors in therapy-related myelodysplasia and acute nonlymphocytic leukemia
-
Pedersen-Bjergaard J, Philip P, Larsen SO, Jensen G, Byrsting K: Chromosome aberrations and prognostic factors in therapy-related myelodysplasia and acute nonlymphocytic leukemia. Blood 76:1083, 1990
-
(1990)
Blood
, vol.76
, pp. 1083
-
-
Pedersen-Bjergaard, J.1
Philip, P.2
Larsen, S.O.3
Jensen, G.4
Byrsting, K.5
-
5
-
-
0021069856
-
The predictive value of initial cytogenetic studies in 148 adults with acute nonlymphocytic leukemia: A 12-year study 1970-1982
-
Larson RA, Le Beau MM, Vardiman JW, Testa JR, Golomb HM, Rowley JD: The predictive value of initial cytogenetic studies in 148 adults with acute nonlymphocytic leukemia: A 12-year study 1970-1982. Cancer Genet Cytogenet 10:219, 1983
-
(1983)
Cancer Genet Cytogenet
, vol.10
, pp. 219
-
-
Larson, R.A.1
Le Beau, M.M.2
Vardiman, J.W.3
Testa, J.R.4
Golomb, H.M.5
Rowley, J.D.6
-
6
-
-
0021264226
-
Fourth International Workshop on Chromosomes in Leukemia, Clinical significance of chromosomal abnormalities in acute nonlymphocytic leukemia
-
Fourth International Workshop on Chromosomes in Leukemia, Clinical significance of chromosomal abnormalities in acute nonlymphocytic leukemia. Cancer Genet Cytogenet 11:332, 1984
-
(1984)
Cancer Genet Cytogenet
, vol.11
, pp. 332
-
-
-
7
-
-
0023838176
-
Specific chromosomal abnormalities in acute nonlymphocytic leukemia correlating with drug susceptibility in vivo
-
Samuels BL, Larson RA, Le Beau MM, Daly KM, Bitter MA, Vardiman JW, Barker CM, Rowley JD, Golomb HM: Specific chromosomal abnormalities in acute nonlymphocytic leukemia correlating with drug susceptibility in vivo. Leukemia 2:79, 1988
-
(1988)
Leukemia
, vol.2
, pp. 79
-
-
Samuels, B.L.1
Larson, R.A.2
Le Beau, M.M.3
Daly, K.M.4
Bitter, M.A.5
Vardiman, J.W.6
Barker, C.M.7
Rowley, J.D.8
Golomb, H.M.9
-
8
-
-
0024501380
-
Prognostic impact of cytogenetic abnormalities in patients with de novo acute nonlymphocytic leukemia
-
Schiffer CA, Lee EJ, Tomiyasu T, Wiernik PH, Testa JR: Prognostic impact of cytogenetic abnormalities in patients with de novo acute nonlymphocytic leukemia. Blood 73:263, 1989
-
(1989)
Blood
, vol.73
, pp. 263
-
-
Schiffer, C.A.1
Lee, E.J.2
Tomiyasu, T.3
Wiernik, P.H.4
Testa, J.R.5
-
9
-
-
0028945753
-
Chromosomal deletions in myelodysplasia
-
Boultwood, J, Fidler C: Chromosomal deletions in myelodysplasia. Leuk Lymphoma 17:71, 1995
-
(1995)
Leuk Lymphoma
, vol.17
, pp. 71
-
-
Boultwood, J.1
Fidler, C.2
-
10
-
-
0027315865
-
Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in myeloid leukemias
-
Le Beau MM, Espinosa III, R, Neuman WL, Stock W, Roulston D, Larson RA, Keinanen M, Westbrook CA: Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in myeloid leukemias. Proc Natl Acad Sci USA 90:5484, 1993
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 5484
-
-
Le Beau, M.M.1
Espinosa III, R.2
Neuman, W.L.3
Stock, W.4
Roulston, D.5
Larson, R.A.6
Keinanen, M.7
Westbrook, C.A.8
-
11
-
-
0028214564
-
Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q-syndrome: Delineation of the critical region on 5q and identification of a 5q- breakpoint
-
Boultwood J, Fidler C, Lewis S, Kelly S, Sheridan H, Littlewood TJ, Buckle VJ, Wainscoat JS: Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q-syndrome: Delineation of the critical region on 5q and identification of a 5q- breakpoint. Genomics 19:425, 1994
-
(1994)
Genomics
, vol.19
, pp. 425
-
-
Boultwood, J.1
Fidler, C.2
Lewis, S.3
Kelly, S.4
Sheridan, H.5
Littlewood, T.J.6
Buckle, V.J.7
Wainscoat, J.S.8
-
12
-
-
0028014297
-
Consistent loss of the D5S89 locus mapping telomeric to the interleukin gene cluster and centromeric to EGR-1 in Patients with 5q- chromosome
-
Nagarajan L, Zavadil J, Claxton D, Lu X, Fairman J, Warrington J, Wasmuth JJ, Chinault AC, Server CE, Slovak ML, Willman CL, Deisseroth AB: Consistent loss of the D5S89 locus mapping telomeric to the interleukin gene cluster and centromeric to EGR-1 in Patients with 5q- chromosome Blood 83:199, 1994
-
(1994)
Blood
, vol.83
, pp. 199
-
-
Nagarajan, L.1
Zavadil, J.2
Claxton, D.3
Lu, X.4
Fairman, J.5
Warrington, J.6
Wasmuth, J.J.7
Chinault, A.C.8
Server, C.E.9
Slovak, M.L.10
Willman, C.L.11
Deisseroth, A.B.12
-
13
-
-
0027724244
-
5q-: Pathogenetic importance of the common deleted region and clinical consequences of the entire deleted segment
-
Pedersen B: 5q-: Pathogenetic importance of the common deleted region and clinical consequences of the entire deleted segment. Anticancer Res 13:1913, 1993
-
(1993)
Anticancer Res
, vol.13
, pp. 1913
-
-
Pedersen, B.1
-
14
-
-
0029142818
-
Physical mapping of the minimal region of loss in 5q- chromosome
-
Fairman J, Chumakov I, Chinault AC, Nowell PC, Nagarajan L: Physical mapping of the minimal region of loss in 5q- chromosome. Proc Natl Acad Sci USA 92:7406, 1995
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 7406
-
-
Fairman, J.1
Chumakov, I.2
Chinault, A.C.3
Nowell, P.C.4
Nagarajan, L.5
-
15
-
-
0026525853
-
Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity from chromosome 5 and 7 in malignant myeloid disorders
-
Richards B, Skoletsky J, Shuber AP, Balfour R, Stern RC, Dorkin HL, Parad RB, Witt D, Klinger KW: Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity from chromosome 5 and 7 in malignant myeloid disorders. Blood 79:1501, 1992
-
(1992)
Blood
, vol.79
, pp. 1501
-
-
Richards, B.1
Skoletsky, J.2
Shuber, A.P.3
Balfour, R.4
Stern, R.C.5
Dorkin, H.L.6
Parad, R.B.7
Witt, D.8
Klinger, K.W.9
-
16
-
-
0027526217
-
Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs
-
Richards B, Skoletsky J, Shuber AP, Balfour R, Stern RC, Dorkin HL, Parad RB, Witt D, Klinger KW: Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs. Hum Mol Genet 2:159, 1993
-
(1993)
Hum Mol Genet
, vol.2
, pp. 159
-
-
Richards, B.1
Skoletsky, J.2
Shuber, A.P.3
Balfour, R.4
Stern, R.C.5
Dorkin, H.L.6
Parad, R.B.7
Witt, D.8
Klinger, K.W.9
-
17
-
-
0000163138
-
Isolation of high molecular-weight DNA from mammalian cells
-
Cold Spring Harbor, NY, Cold Spring Harbor Laboratory
-
Sambrook J, Fritch ER, Maniatis T: Isolation of high molecular-weight DNA from mammalian cells, in Molecular Cloning: A laboratory Manual (ed 2). Cold Spring Harbor, NY, Cold Spring Harbor Laboratory, 1989, p 9.14
-
(1989)
Molecular Cloning: A Laboratory Manual (Ed 2)
, pp. 914
-
-
Sambrook, J.1
Fritch, E.R.2
Maniatis, T.3
-
18
-
-
0028865860
-
A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps
-
Sheffield VC, Weber JL, Buetow KH, Murray JC, Even DA, Wiles K, Gastier JM, Pulido JC, Yandava C, Sunden SL, Mattes G, Businga T, McClain A, Beck J, Scherpier T, Gilliam J, Zhong J, Duyk GM: A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Hum Mol Genet 4:1837, 1995
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1837
-
-
Sheffield, V.C.1
Weber, J.L.2
Buetow, K.H.3
Murray, J.C.4
Even, D.A.5
Wiles, K.6
Gastier, J.M.7
Pulido, J.C.8
Yandava, C.9
Sunden, S.L.10
Mattes, G.11
Businga, T.12
McClain, A.13
Beck, J.14
Scherpier, T.15
Gilliam, J.16
Zhong, J.17
Duyk, G.M.18
-
19
-
-
0028231090
-
The 1993-4 Genethon human genetic linkage map
-
Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, Lathrop M, Weissenbach J: The 1993-4 Genethon human genetic linkage map. Nat Genet 7:246, 1994
-
(1994)
Nat Genet
, vol.7
, pp. 246
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Millasseau, P.6
Marc, S.7
Lathrop, M.8
Weissenbach, J.9
-
20
-
-
0026422099
-
Dinucleotide repeat polymorphism the human interleukin 9 gene
-
Polymeropoulos MH, Xiao H, Rath DS, Merril CR: Dinucleotide repeat polymorphism the human interleukin 9 gene. Nucleic Acids Res 19:688, 1991
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 688
-
-
Polymeropoulos, M.H.1
Xiao, H.2
Rath, D.S.3
Merril, C.R.4
-
21
-
-
10144236231
-
-
unpublished data. Whitehead Institute/MIT Center for Genome Research, Human Genetic Mapping Project
-
Weissenbach J, unpublished data. Whitehead Institute/MIT Center for Genome Research, Human Genetic Mapping Project
-
-
-
Weissenbach, J.1
-
22
-
-
0029163591
-
A collection of ordered tetranucleotide-repeat markers from the human genome
-
The Utah Marker Development Group, A collection of ordered tetranucleotide-repeat markers from the human genome. Am J Hum Genet 57:619, 1995
-
(1995)
Am J Hum Genet
, vol.57
, pp. 619
-
-
-
23
-
-
0027533768
-
Myeloid but not lymphoid cells carry the 5q deletion: Polymerase chain reaction analysis of loss of heterozygosity using mini-repeat sequences on highly purified cell fractions
-
Kroef MJ, Fibbe WE, Mout R, Jansen RPM, Haak HL, Wessels JW, Van Kamp H, Willemze R, Landegent JE: Myeloid but not lymphoid cells carry the 5q deletion: Polymerase chain reaction analysis of loss of heterozygosity using mini-repeat sequences on highly purified cell fractions. Blood 81:1849, 1993
-
(1993)
Blood
, vol.81
, pp. 1849
-
-
Kroef, M.J.1
Fibbe, W.E.2
Mout, R.3
Jansen, R.P.M.4
Haak, H.L.5
Wessels, J.W.6
Van Kamp, H.7
Willemze, R.8
Landegent, J.E.9
|