-
1
-
-
0037458629
-
LOT1 (PLAGL1/ZAC1), the candidate tumor suppressor gene at chromosome 6q24-25, is epigenetically regulated in cancer
-
Abdollahi A., Pisarcik D., Roberts D., Weinstein J., Cairns P., and Hamilton T.C. LOT1 (PLAGL1/ZAC1), the candidate tumor suppressor gene at chromosome 6q24-25, is epigenetically regulated in cancer. J. Biol. Chem. 278 (2003) 6041-6049
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 6041-6049
-
-
Abdollahi, A.1
Pisarcik, D.2
Roberts, D.3
Weinstein, J.4
Cairns, P.5
Hamilton, T.C.6
-
2
-
-
25444522966
-
The candidate tumor suppressor gene ZAC is involved in keratinocyte differentiation and its expression is lost in basal cell carcinomas
-
Basyuk E., Coulon V., Le Digarcher A., Coisy-Quivy M., Moles J.P., Gandarillas A., and Journot L. The candidate tumor suppressor gene ZAC is involved in keratinocyte differentiation and its expression is lost in basal cell carcinomas. Mol. Cancer Res. 3 (2005) 483-492
-
(2005)
Mol. Cancer Res.
, vol.3
, pp. 483-492
-
-
Basyuk, E.1
Coulon, V.2
Le Digarcher, A.3
Coisy-Quivy, M.4
Moles, J.P.5
Gandarillas, A.6
Journot, L.7
-
3
-
-
0024354518
-
Mutations in human breast cancer: An overview
-
Callahan R., and Campbell G. Mutations in human breast cancer: An overview. J. Natl. Cancer Inst. 81 (1989) 1780-1786
-
(1989)
J. Natl. Cancer Inst.
, vol.81
, pp. 1780-1786
-
-
Callahan, R.1
Campbell, G.2
-
4
-
-
0038732456
-
Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27
-
Cesari R., Martin E.S., Calin G.A., Pentimalli F., Bichi R., McAdams H., Trapasso F., Drusco A., Shimizu M., Masciullo V., D'Andrilli G., Scambia G., Picchio M.C., Alder H., Godwin A.K., and Croce C.M. Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27. Proc. Natl. Acad. Sci. USA 100 (2003) 5956-5961
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 5956-5961
-
-
Cesari, R.1
Martin, E.S.2
Calin, G.A.3
Pentimalli, F.4
Bichi, R.5
McAdams, H.6
Trapasso, F.7
Drusco, A.8
Shimizu, M.9
Masciullo, V.10
D'Andrilli, G.11
Scambia, G.12
Picchio, M.C.13
Alder, H.14
Godwin, A.K.15
Croce, C.M.16
-
5
-
-
0025832422
-
Allelotype of human breast carcinoma: A second major site for loss of heterozygosity is on chromosome 6q
-
Devilee P., van Vliet M., van Sloun P., Kuipers Dijkshoorn N., Hermans J., Pearson P.L., and Cornelisse C.J. Allelotype of human breast carcinoma: A second major site for loss of heterozygosity is on chromosome 6q. Oncogene 6 (1991) 1705-1711
-
(1991)
Oncogene
, vol.6
, pp. 1705-1711
-
-
Devilee, P.1
van Vliet, M.2
van Sloun, P.3
Kuipers Dijkshoorn, N.4
Hermans, J.5
Pearson, P.L.6
Cornelisse, C.J.7
-
6
-
-
0035740250
-
Chromosomal deletions and tumor suppressor genes in prostate cancer
-
Dong J.T. Chromosomal deletions and tumor suppressor genes in prostate cancer. Cancer Metastasis Rev. 20 (2001) 173-193
-
(2001)
Cancer Metastasis Rev.
, vol.20
, pp. 173-193
-
-
Dong, J.T.1
-
7
-
-
0034660852
-
Deletion at 13q21 is associated with aggressive prostate cancers
-
Dong J.T., Chen C., Stultz B.G., Isaacs J.T., and Frierson Jr. H.F. Deletion at 13q21 is associated with aggressive prostate cancers. Cancer Res. 60 (2000) 3880-3883
-
(2000)
Cancer Res.
, vol.60
, pp. 3880-3883
-
-
Dong, J.T.1
Chen, C.2
Stultz, B.G.3
Isaacs, J.T.4
Frierson Jr., H.F.5
-
8
-
-
33746930170
-
FOXO1A is a candidate for the 13q14 tumor suppressor gene inhibiting androgen receptor signaling in prostate cancer
-
Dong X.Y., Chen C., Sun X., Guo P., Vessella R.L., Wang R.X., Chung L.W., Zhou W., and Dong J.T. FOXO1A is a candidate for the 13q14 tumor suppressor gene inhibiting androgen receptor signaling in prostate cancer. Cancer Res. 66 (2006) 6998-7006
-
(2006)
Cancer Res.
, vol.66
, pp. 6998-7006
-
-
Dong, X.Y.1
Chen, C.2
Sun, X.3
Guo, P.4
Vessella, R.L.5
Wang, R.X.6
Chung, L.W.7
Zhou, W.8
Dong, J.T.9
-
9
-
-
41149126821
-
SnoRNA U50 is a candidate tumor-suppressor gene at 6q14.3 with a mutation associated with clinically significant prostate cancer
-
Dong X.Y., Rodriguez C., Guo P., Sun X., Talbot J.T., Zhou W., Petros J., Li Q., Vessella R.L., Kibel A.S., Stevens V.L., Calle E.E., and Dong J.T. SnoRNA U50 is a candidate tumor-suppressor gene at 6q14.3 with a mutation associated with clinically significant prostate cancer. Hum. Mol. Genet. 17 (2008) 1031-1042
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 1031-1042
-
-
Dong, X.Y.1
Rodriguez, C.2
Guo, P.3
Sun, X.4
Talbot, J.T.5
Zhou, W.6
Petros, J.7
Li, Q.8
Vessella, R.L.9
Kibel, A.S.10
Stevens, V.L.11
Calle, E.E.12
Dong, J.T.13
-
10
-
-
0025166061
-
Characterization of chromosomal anomalies in human breast cancer. A comparison of 30 paradiploid cases with few chromosome changes
-
Dutrillaux B., Gerbault-Seureau M., and Zafrani B. Characterization of chromosomal anomalies in human breast cancer. A comparison of 30 paradiploid cases with few chromosome changes. Cancer Genet. Cytogenet. 49 (1990) 203-217
-
(1990)
Cancer Genet. Cytogenet.
, vol.49
, pp. 203-217
-
-
Dutrillaux, B.1
Gerbault-Seureau, M.2
Zafrani, B.3
-
11
-
-
0027408255
-
Frequent loss of heterozygosity on chromosome 6 in human ovarian carcinoma
-
Foulkes W.D., Ragoussis J., Stamp G.W., Allan G.J., and Trowsdale J. Frequent loss of heterozygosity on chromosome 6 in human ovarian carcinoma. Br. J. Cancer 67 (1993) 551-559
-
(1993)
Br. J. Cancer
, vol.67
, pp. 551-559
-
-
Foulkes, W.D.1
Ragoussis, J.2
Stamp, G.W.3
Allan, G.J.4
Trowsdale, J.5
-
12
-
-
41949142377
-
Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33
-
Gold B., Kirchhoff T., Stefanov S., Lautenberger J., Viale A., Garber J., Friedman E., Narod S., Olshen A.B., Gregersen P., Kosarin K., Olsh A., Bergeron J., Ellis N.A., Klein R.J., Clark A.G., Norton L., Dean M., Boyd J., and Offit K. Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33. Proc. Natl. Acad. Sci. USA 105 (2008) 4340-4345
-
(2008)
Proc. Natl. Acad. Sci. USA
, vol.105
, pp. 4340-4345
-
-
Gold, B.1
Kirchhoff, T.2
Stefanov, S.3
Lautenberger, J.4
Viale, A.5
Garber, J.6
Friedman, E.7
Narod, S.8
Olshen, A.B.9
Gregersen, P.10
Kosarin, K.11
Olsh, A.12
Bergeron, J.13
Ellis, N.A.14
Klein, R.J.15
Clark, A.G.16
Norton, L.17
Dean, M.18
Boyd, J.19
Offit, K.20
more..
-
13
-
-
33646546654
-
Genomic alterations identified by array comparative genomic hybridization as prognostic markers in tamoxifen-treated estrogen receptor-positive breast cancer
-
Han W., Han M.R., Kang J.J., Bae J.Y., Lee J.H., Bae Y.J., Lee J.E., Shin H.J., Hwang K.T., Hwang S.E., Kim S.W., and Noh D.Y. Genomic alterations identified by array comparative genomic hybridization as prognostic markers in tamoxifen-treated estrogen receptor-positive breast cancer. BMC Cancer 6 (2006) 92
-
(2006)
BMC Cancer
, vol.6
, pp. 92
-
-
Han, W.1
Han, M.R.2
Kang, J.J.3
Bae, J.Y.4
Lee, J.H.5
Bae, Y.J.6
Lee, J.E.7
Shin, H.J.8
Hwang, K.T.9
Hwang, S.E.10
Kim, S.W.11
Noh, D.Y.12
-
14
-
-
30844442607
-
The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C
-
Kishore S., and Stamm S. The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C. Science 311 (2006) 230-232
-
(2006)
Science
, vol.311
, pp. 230-232
-
-
Kishore, S.1
Stamm, S.2
-
15
-
-
0032887168
-
DNA copy number losses in human neoplasms
-
Knuutila S., Aalto Y., Autio K., Bjorkqvist A.M., El-Rifai W., Hemmer S., Huhta T., Kettunen E., Kiuru-Kuhlefelt S., Larramendy M.L., Lushnikova T., Monni O., Pere H., Tapper J., Tarkkanen M., Varis A., Wasenius V.M., Wolf M., and Zhu Y. DNA copy number losses in human neoplasms. Am. J. Pathol. 155 (1999) 683-694
-
(1999)
Am. J. Pathol.
, vol.155
, pp. 683-694
-
-
Knuutila, S.1
Aalto, Y.2
Autio, K.3
Bjorkqvist, A.M.4
El-Rifai, W.5
Hemmer, S.6
Huhta, T.7
Kettunen, E.8
Kiuru-Kuhlefelt, S.9
Larramendy, M.L.10
Lushnikova, T.11
Monni, O.12
Pere, H.13
Tapper, J.14
Tarkkanen, M.15
Varis, A.16
Wasenius, V.M.17
Wolf, M.18
Zhu, Y.19
-
16
-
-
0025321563
-
Frequent loss of heterozygosity on chromosomes 6q, 11, and 17 in human ovarian carcinomas
-
Lee J.H., Kavanagh J.J., Wildrick D.M., Wharton J.T., and Blick M. Frequent loss of heterozygosity on chromosomes 6q, 11, and 17 in human ovarian carcinomas. Cancer Res. 50 (1990) 2724-2728
-
(1990)
Cancer Res.
, vol.50
, pp. 2724-2728
-
-
Lee, J.H.1
Kavanagh, J.J.2
Wildrick, D.M.3
Wharton, J.T.4
Blick, M.5
-
17
-
-
34548701788
-
UTRN on chromosome 6q24 is mutated in multiple tumors
-
Li Y., Huang J., Zhao Y.L., He J., Wang W., Davies K.E., Nose V., and Xiao S. UTRN on chromosome 6q24 is mutated in multiple tumors. Oncogene 26 (2007) 6220-6228
-
(2007)
Oncogene
, vol.26
, pp. 6220-6228
-
-
Li, Y.1
Huang, J.2
Zhao, Y.L.3
He, J.4
Wang, W.5
Davies, K.E.6
Nose, V.7
Xiao, S.8
-
18
-
-
33847187076
-
Non-coding RNAs: Lessons from the small nuclear and small nucleolar RNAs
-
Matera A.G., Terns R.M., and Terns M.P. Non-coding RNAs: Lessons from the small nuclear and small nucleolar RNAs. Nat. Rev. Mol. Cell Biol. 8 (2007) 209-220
-
(2007)
Nat. Rev. Mol. Cell Biol.
, vol.8
, pp. 209-220
-
-
Matera, A.G.1
Terns, R.M.2
Terns, M.P.3
-
19
-
-
1842584883
-
RNA regulation: A new genetics?
-
Mattick J.S. RNA regulation: A new genetics?. Nat. Rev. Genet. 5 (2004) 316-323
-
(2004)
Nat. Rev. Genet.
, vol.5
, pp. 316-323
-
-
Mattick, J.S.1
-
21
-
-
0030825508
-
Chromosomal imbalance maps of malignant solid tumors: A cytogenetic survey of 3185 neoplasms
-
Mertens F., Johansson B., Hoglund M., and Mitelman F. Chromosomal imbalance maps of malignant solid tumors: A cytogenetic survey of 3185 neoplasms. Cancer Res. 57 (1997) 2765-2780
-
(1997)
Cancer Res.
, vol.57
, pp. 2765-2780
-
-
Mertens, F.1
Johansson, B.2
Hoglund, M.3
Mitelman, F.4
-
22
-
-
0034546548
-
Molecular analysis of the h-warts/LATS1 gene in human breast cancer
-
Morinaga N., Shitara Y., Yanagita Y., Koida T., Kimura M., Asao T., Kimijima I., Takenoshita S., Hirota T., Saya H., and Kuwano H. Molecular analysis of the h-warts/LATS1 gene in human breast cancer. Int. J. Oncol. 17 (2000) 1125-1129
-
(2000)
Int. J. Oncol.
, vol.17
, pp. 1125-1129
-
-
Morinaga, N.1
Shitara, Y.2
Yanagita, Y.3
Koida, T.4
Kimura, M.5
Asao, T.6
Kimijima, I.7
Takenoshita, S.8
Hirota, T.9
Saya, H.10
Kuwano, H.11
-
23
-
-
58249098615
-
GAS5, a non-protein-coding RNA, controls apoptosis and is downregulated in breast cancer
-
Mourtada-Maarabouni M., Pickard M.R., Hedge V.L., Farzaneh F., and Williams G.T. GAS5, a non-protein-coding RNA, controls apoptosis and is downregulated in breast cancer. Oncogene 28 (2009) 195-208
-
(2009)
Oncogene
, vol.28
, pp. 195-208
-
-
Mourtada-Maarabouni, M.1
Pickard, M.R.2
Hedge, V.L.3
Farzaneh, F.4
Williams, G.T.5
-
24
-
-
0030223060
-
Loss of heterozygosity on the long arm of chromosome 6 in breast cancer: Possibly four regions of deletion
-
Noviello C., Courjal F., and Theillet C. Loss of heterozygosity on the long arm of chromosome 6 in breast cancer: Possibly four regions of deletion. Clin. Cancer Res. 2 (1996) 1601-1606
-
(1996)
Clin. Cancer Res.
, vol.2
, pp. 1601-1606
-
-
Noviello, C.1
Courjal, F.2
Theillet, C.3
-
25
-
-
0028855714
-
Proximal 6q, a region showing allele loss in primary breast cancer
-
Orphanos V., McGown G., Hey Y., Boyle J.M., and Santibanez- Koref M. Proximal 6q, a region showing allele loss in primary breast cancer. Br. J. Cancer 71 (1995) 290-293
-
(1995)
Br. J. Cancer
, vol.71
, pp. 290-293
-
-
Orphanos, V.1
McGown, G.2
Hey, Y.3
Boyle, J.M.4
Santibanez- Koref, M.5
-
26
-
-
0033990756
-
At least five regions of imbalance on 6q in breast tumors, combining losses and gains
-
Rodriguez C., Causse A., Ursule E., and Theillet C. At least five regions of imbalance on 6q in breast tumors, combining losses and gains. Genes Chromosomes Cancer 27 (2000) 76-84
-
(2000)
Genes Chromosomes Cancer
, vol.27
, pp. 76-84
-
-
Rodriguez, C.1
Causse, A.2
Ursule, E.3
Theillet, C.4
-
27
-
-
62649100810
-
Genome- wide linkage scan reveals three putative breast-cancer-susceptibility loci
-
Rosa-Rosa J.M., Pita G., Urioste M., Llort G., Brunet J., Lazaro C., Blanco I., Ramon Y.C.T., Diez O., de la Hoya M., Caldes T., Tejada M.I., Gonzalez-Neira A., and Benitez J. Genome- wide linkage scan reveals three putative breast-cancer-susceptibility loci. Am. J. Hum. Genet. 84 (2009) 115-122
-
(2009)
Am. J. Hum. Genet.
, vol.84
, pp. 115-122
-
-
Rosa-Rosa, J.M.1
Pita, G.2
Urioste, M.3
Llort, G.4
Brunet, J.5
Lazaro, C.6
Blanco, I.7
Ramon, Y.C.T.8
Diez, O.9
de la Hoya, M.10
Caldes, T.11
Tejada, M.I.12
Gonzalez-Neira, A.13
Benitez, J.14
-
28
-
-
0030042705
-
A gene on 6q 14-21 restores senescence to immortal ovarian tumor cells
-
Sandhu A.K., Kaur G.P., Reddy D.E., Rane N.S., and Athwal R.S. A gene on 6q 14-21 restores senescence to immortal ovarian tumor cells. Oncogene 12 (1996) 247-252
-
(1996)
Oncogene
, vol.12
, pp. 247-252
-
-
Sandhu, A.K.1
Kaur, G.P.2
Reddy, D.E.3
Rane, N.S.4
Athwal, R.S.5
-
29
-
-
0031714495
-
Chromosome alterations in breast carcinomas: Frequent involvement of DNA losses including chromosomes 4q and 21q
-
Schwendel A., Richard F., Langreck H., Kaufmann O., Lage H., Winzer K.J., Petersen I., and Dietel M. Chromosome alterations in breast carcinomas: Frequent involvement of DNA losses including chromosomes 4q and 21q. Br. J. Cancer 78 (1998) 806-811
-
(1998)
Br. J. Cancer
, vol.78
, pp. 806-811
-
-
Schwendel, A.1
Richard, F.2
Langreck, H.3
Kaufmann, O.4
Lage, H.5
Winzer, K.J.6
Petersen, I.7
Dietel, M.8
-
30
-
-
0035399798
-
Clinical relevance of genomic aberrations in homogeneously treated high-risk stage II/III breast cancer patients
-
Seute A., Sinn H.P., Schlenk R.F., Emig R., Wallwiener D., Grischke E.M., Hohaus S., Dohner H., Haas R., and Bentz M. Clinical relevance of genomic aberrations in homogeneously treated high-risk stage II/III breast cancer patients. Int. J. Cancer 93 (2001) 80-84
-
(2001)
Int. J. Cancer
, vol.93
, pp. 80-84
-
-
Seute, A.1
Sinn, H.P.2
Schlenk, R.F.3
Emig, R.4
Wallwiener, D.5
Grischke, E.M.6
Hohaus, S.7
Dohner, H.8
Haas, R.9
Bentz, M.10
-
31
-
-
0030050690
-
Multiple regions of chromosome 6q affected by loss of heterozygosity in primary human breast carcinomas
-
Sheng Z.M., Marchetti A., Buttitta F., Champeme M.H., Campani D., Bistocchi M., Lidereau R., and Callahan R. Multiple regions of chromosome 6q affected by loss of heterozygosity in primary human breast carcinomas. Br. J. Cancer 73 (1996) 144-147
-
(1996)
Br. J. Cancer
, vol.73
, pp. 144-147
-
-
Sheng, Z.M.1
Marchetti, A.2
Buttitta, F.3
Champeme, M.H.4
Campani, D.5
Bistocchi, M.6
Lidereau, R.7
Callahan, R.8
-
32
-
-
0031756336
-
Classification of gas5 as a multi-small-nucleolar-RNA (snoRNA) host gene and a member of the 5(-terminal oligopyrimidine gene family reveals common features of snoRNA host genes
-
Smith C.M., and Steitz J.A. Classification of gas5 as a multi-small-nucleolar-RNA (snoRNA) host gene and a member of the 5(-terminal oligopyrimidine gene family reveals common features of snoRNA host genes. Mol. Cell. Biol. 18 (1998) 6897-6909
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 6897-6909
-
-
Smith, C.M.1
Steitz, J.A.2
-
33
-
-
34047233628
-
Cancer screening in the United States, 2007: A review of current guidelines, practices, and prospects
-
Smith R.A., Cokkinides V., and Eyre H.J. Cancer screening in the United States, 2007: A review of current guidelines, practices, and prospects. CA. Cancer J. Clin. 57 (2007) 90-104
-
(2007)
CA. Cancer J. Clin.
, vol.57
, pp. 90-104
-
-
Smith, R.A.1
Cokkinides, V.2
Eyre, H.J.3
-
34
-
-
20144389099
-
Frequent somatic mutations of the transcription factor ATBF1 in human prostate cancer
-
Sun X., Frierson H.F., Chen C., Li C., Ran Q., Otto K.B., Cantarel B.L., Vessella R.L., Gao A.C., Petros J., Miura Y., Simons J.W., and Dong J.T. Frequent somatic mutations of the transcription factor ATBF1 in human prostate cancer. Nat. Genet. 37 (2005) 407-412
-
(2005)
Nat. Genet.
, vol.37
, pp. 407-412
-
-
Sun, X.1
Frierson, H.F.2
Chen, C.3
Li, C.4
Ran, Q.5
Otto, K.B.6
Cantarel, B.L.7
Vessella, R.L.8
Gao, A.C.9
Petros, J.10
Miura, Y.11
Simons, J.W.12
Dong, J.T.13
-
35
-
-
9544220641
-
A defined chromosome 6q fragment (at D6S310) harbors a putative tumor suppressor gene for breast cancer
-
Theile M., Seitz S., Arnold W., Jandrig B., Frege R., Schlag P.M., Haensch W., Guski H., Winzer K.J., Barrett J.C., and Scherneck S. A defined chromosome 6q fragment (at D6S310) harbors a putative tumor suppressor gene for breast cancer. Oncogene 13 (1996) 677-685
-
(1996)
Oncogene
, vol.13
, pp. 677-685
-
-
Theile, M.1
Seitz, S.2
Arnold, W.3
Jandrig, B.4
Frege, R.5
Schlag, P.M.6
Haensch, W.7
Guski, H.8
Winzer, K.J.9
Barrett, J.C.10
Scherneck, S.11
-
36
-
-
0032555068
-
hZAC encodes a zinc finger protein with antiproliferative properties and maps to a chromosomal region frequently lost in cancer
-
Varrault A., Ciani E., Apiou F., Bilanges B., Hoffmann A., Pantaloni C., Bockaert J., Spengler D., and Journot L. hZAC encodes a zinc finger protein with antiproliferative properties and maps to a chromosomal region frequently lost in cancer. Proc. Natl. Acad. Sci. USA 95 (1998) 8835-8840
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 8835-8840
-
-
Varrault, A.1
Ciani, E.2
Apiou, F.3
Bilanges, B.4
Hoffmann, A.5
Pantaloni, C.6
Bockaert, J.7
Spengler, D.8
Journot, L.9
-
37
-
-
0038021119
-
SASH1: A candidate tumor suppressor gene on chromosome 6q24.3 is downregulated in breast cancer
-
Zeller C., Hinzmann B., Seitz S., Prokoph H., Burkhard-Goettges E., Fischer J., Jandrig B., Schwarz L.E., Rosenthal A., and Scherneck S. SASH1: A candidate tumor suppressor gene on chromosome 6q24.3 is downregulated in breast cancer. Oncogene 22 (2003) 2972-2983
-
(2003)
Oncogene
, vol.22
, pp. 2972-2983
-
-
Zeller, C.1
Hinzmann, B.2
Seitz, S.3
Prokoph, H.4
Burkhard-Goettges, E.5
Fischer, J.6
Jandrig, B.7
Schwarz, L.E.8
Rosenthal, A.9
Scherneck, S.10
-
38
-
-
0032420650
-
Detection of 6q deletions in breast carcinoma cell lines by fluorescence in situ hybridization
-
Zhang Y., Matthiesen P., Siebert R., Harder S., Theile M., Scherneck S., and Schlegelberger B. Detection of 6q deletions in breast carcinoma cell lines by fluorescence in situ hybridization. Hum. Genet. 103 (1998) 727-729
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(1998)
Hum. Genet.
, vol.103
, pp. 727-729
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Zhang, Y.1
Matthiesen, P.2
Siebert, R.3
Harder, S.4
Theile, M.5
Scherneck, S.6
Schlegelberger, B.7
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