-
1
-
-
0029090221
-
Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)
-
Ahn J., Lüdecke H., Lindow S., Horton W. A., Lee B., Wagner M. J., Horsthemke B., Wells D. E. Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1). Nature Genet. 11:1995;137-143.
-
(1995)
Nature Genet.
, vol.11
, pp. 137-143
-
-
Ahn, J.1
Lüdecke, H.2
Lindow, S.3
Horton, W.A.4
Lee, B.5
Wagner, M.J.6
Horsthemke, B.7
Wells, D.E.8
-
3
-
-
0024320151
-
Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p
-
Bale S. J., Dracopoli N. C., Tucker M. A., Clark W. H., Fraser M. C., Stanger B. Z., Green P., Donis-Keller H., Housman D. E., Greene M. H. Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p. N. Engl. J. Med. 320:1989;1367-1372.
-
(1989)
N. Engl. J. Med.
, vol.320
, pp. 1367-1372
-
-
Bale, S.J.1
Dracopoli, N.C.2
Tucker, M.A.3
Clark, W.H.4
Fraser, M.C.5
Stanger, B.Z.6
Green, P.7
Donis-Keller, H.8
Housman, D.E.9
Greene, M.H.10
-
4
-
-
0030006019
-
Hereditary multiple exostoses: Confirmation of linkage to chromosomes 8 and 11
-
Blanton S. H., Hogue D., Wagner M., Wells D., Young I. D., Hecht J. T. Hereditary multiple exostoses: Confirmation of linkage to chromosomes 8 and 11. Am. J. Med. Genet. 62:1996;150-159.
-
(1996)
Am. J. Med. Genet.
, vol.62
, pp. 150-159
-
-
Blanton, S.H.1
Hogue, D.2
Wagner, M.3
Wells, D.4
Young, I.D.5
Hecht, J.T.6
-
5
-
-
0027422876
-
Biological and clinical significance of cytogenetic and molecular cytogenetic abnormalities in benign and malignant cartilaginous lesions
-
Bridge J. A., Parmajit S. B., Anderson J. R., Neff J. R. Biological and clinical significance of cytogenetic and molecular cytogenetic abnormalities in benign and malignant cartilaginous lesions. Cancer Genet. Cytogenet. 69:1993;79-90.
-
(1993)
Cancer Genet. Cytogenet.
, vol.69
, pp. 79-90
-
-
Bridge, J.A.1
Parmajit, S.B.2
Anderson, J.R.3
Neff, J.R.4
-
6
-
-
0028926888
-
Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: One probably imprinted, another associated with N-myc amplification
-
Caron H., Peter M., Van Sluis P., Speleman F., De Kraker J., Laureys G., Michon J., Brugieres L., Voute P. A., Westerveld A., Slater R., Delattre O., Versteeg R. Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: One probably imprinted, another associated with N-myc amplification. Hum. Mol. Genet. 4:1995;535-539.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 535-539
-
-
Caron, H.1
Peter, M.2
Van Sluis, P.3
Speleman, F.4
De Kraker, J.5
Laureys, G.6
Michon, J.7
Brugieres, L.8
Voute, P.A.9
Westerveld, A.10
Slater, R.11
Delattre, O.12
Versteeg, R.13
-
7
-
-
0027366989
-
Genetic heterogeneity in families with hereditary multiple exostoses
-
Cook A., Raskind W., Blanton S. H., Pauli R. M., Gregg R. G., Francomano C. A., Puffenberger E., Conrad E. U., Schmale G., Schellenberg G., Wijsman E., Hecht J. T., Wells D., Wagner M. J. Genetic heterogeneity in families with hereditary multiple exostoses. Am. J. Hum. Genet. 53:1993;71-79.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 71-79
-
-
Cook, A.1
Raskind, W.2
Blanton, S.H.3
Pauli, R.M.4
Gregg, R.G.5
Francomano, C.A.6
Puffenberger, E.7
Conrad, E.U.8
Schmale, G.9
Schellenberg, G.10
Wijsman, E.11
Hecht, J.T.12
Wells, D.13
Wagner, M.J.14
-
8
-
-
0027363063
-
Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse
-
Dietrich W. F., Lander E. S., Smith J. S., Moser A. R., Gould K. A., Luongo C., Borenstein N., Dove W. Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse. Cell. 75:1993;631-639.
-
(1993)
Cell
, vol.75
, pp. 631-639
-
-
Dietrich, W.F.1
Lander, E.S.2
Smith, J.S.3
Moser, A.R.4
Gould, K.A.5
Luongo, C.6
Borenstein, N.7
Dove, W.8
-
9
-
-
0029259085
-
Maximum discrimination hidden Markov models of sequence consensus
-
Eddy S. R., Mitchison G., Durbin R. Maximum discrimination hidden Markov models of sequence consensus. J. Comput. Biol. 2:1995;9-23.
-
(1995)
J. Comput. Biol.
, vol.2
, pp. 9-23
-
-
Eddy, S.R.1
Mitchison, G.2
Durbin, R.3
-
10
-
-
0027231756
-
Cervical cord compression in hereditary multiple exostoses
-
Eder H. G., Oberbauer R. W., Ranner G. Cervical cord compression in hereditary multiple exostoses. J. Neurosurg. Sci. 37:1993;53-56.
-
(1993)
J. Neurosurg. Sci.
, vol.37
, pp. 53-56
-
-
Eder, H.G.1
Oberbauer, R.W.2
Ranner, G.3
-
11
-
-
0030218799
-
Finding genes by computer: The state of the art
-
Fickett J. W. Finding genes by computer: The state of the art. Trends Genet. 12:1996;316-320.
-
(1996)
Trends Genet.
, vol.12
, pp. 316-320
-
-
Fickett, J.W.1
-
13
-
-
0028917663
-
Hereditary multiple exostosis and chondrosarcoma: Linkage to chromosome 11 and loss of heterozygosity for EXT-linked markers on chromosome 11 and 8
-
Hecht J. T., Hogue D., Strong L. C., Hansen M. F., Blanton S. H., Wagner M. Hereditary multiple exostosis and chondrosarcoma: Linkage to chromosome 11 and loss of heterozygosity for EXT-linked markers on chromosome 11 and 8. Am. J. Hum. Genet. 56:1995;1125-1131.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 1125-1131
-
-
Hecht, J.T.1
Hogue, D.2
Strong, L.C.3
Hansen, M.F.4
Blanton, S.H.5
Wagner, M.6
-
14
-
-
0019966986
-
Chromosomal localization of human cellular homologues of two viral oncogenes
-
Heisterkamp N., Groffen J., Stephenson J. R., Spurr N. K., Goodfellow P. N., Solomon E., Carrit B., Bodmer W. F. Chromosomal localization of human cellular homologues of two viral oncogenes. Nature. 299:1982;747-749.
-
(1982)
Nature
, vol.299
, pp. 747-749
-
-
Heisterkamp, N.1
Groffen, J.2
Stephenson, J.R.3
Spurr, N.K.4
Goodfellow, P.N.5
Solomon, E.6
Carrit, B.7
Bodmer, W.F.8
-
15
-
-
0025810316
-
Hereditary multiple exostoses
-
Hennekam R. C. M. Hereditary multiple exostoses. J. Med. Genet. 28:1991;262-266.
-
(1991)
J. Med. Genet.
, vol.28
, pp. 262-266
-
-
Hennekam, R.C.M.1
-
16
-
-
0342464747
-
Mutational analysis of hereditary multiple exostoses
-
Hogue D. A., Clines G., Lovett M., Hansen M. F., Hecht J. T. Mutational analysis of hereditary multiple exostoses. Am. J. Hum. Genet. 56:1996;A1521.
-
(1996)
Am. J. Hum. Genet.
, vol.56
, pp. 1521
-
-
Hogue, D.A.1
Clines, G.2
Lovett, M.3
Hansen, M.F.4
Hecht, J.T.5
-
17
-
-
13344249759
-
BRCA1 is secreted and exhibits properties of a granin
-
Jensen R. A., Thompson M. E., Jetton T. L., Szabo C. I., van der Meer R., Helou B., Tronick S. R., Page D. L., King M.-C., Holt J. T. BRCA1 is secreted and exhibits properties of a granin. Nature Genet. 12:1996;303-308.
-
(1996)
Nature Genet.
, vol.12
, pp. 303-308
-
-
Jensen, R.A.1
Thompson, M.E.2
Jetton, T.L.3
Szabo, C.I.4
Van Der Meer, R.5
Helou, B.6
Tronick, S.R.7
Page, D.L.8
King, M.-C.9
Holt, J.T.10
-
18
-
-
0029025442
-
Cytogenetic analysis of the short-term cultured squamous cell carcinomas of the lung
-
Johansson M., Jin Y., Mandahl N., Hambraeus G., Johansson L., Mittelman F., Heim S. Cytogenetic analysis of the short-term cultured squamous cell carcinomas of the lung. Cancer Genet. Cytogenet. 81:1995;46-55.
-
(1995)
Cancer Genet. Cytogenet.
, vol.81
, pp. 46-55
-
-
Johansson, M.1
Jin, Y.2
Mandahl, N.3
Hambraeus, G.4
Johansson, L.5
Mittelman, F.6
Heim, S.7
-
19
-
-
0029065726
-
Development of a panel of monochromosomal somatic cell hybrids for rapid gene mapping
-
Kelsall D. P., Rooke L., Warne D., Bonzyk M., Cullin L., Cox S., West L., Povey S., Spurr N. K. Development of a panel of monochromosomal somatic cell hybrids for rapid gene mapping. Ann. Hum. Genet. 59:1995;233-241.
-
(1995)
Ann. Hum. Genet.
, vol.59
, pp. 233-241
-
-
Kelsall, D.P.1
Rooke, L.2
Warne, D.3
Bonzyk, M.4
Cullin, L.5
Cox, S.6
West, L.7
Povey, S.8
Spurr, N.K.9
-
20
-
-
0025792297
-
Structural features in eukaryotic mRNAs that modulate the initiation of translation
-
Kozak M. Structural features in eukaryotic mRNAs that modulate the initiation of translation. J. Biol. Chem. 266:1991;19867-19870.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 19867-19870
-
-
Kozak, M.1
-
21
-
-
0002345846
-
Genetic and physical mapping
-
Cold Spring Harbor: Cold Spring Harbor Laboratory Press. p. 39-81
-
Lehrach H. Genetic and physical mapping. Genome Analysis. 1990;Cold Spring Harbor Laboratory Press, Cold Spring Harbor. p. 39-81.
-
(1990)
Genome Analysis
-
-
Lehrach, H.1
-
22
-
-
0028351625
-
A gene for hereditary multiple exostoses maps to chromosome 19p
-
Le Merrer M., Legeai-Mallet L., Jeannin P. M., Horsthemke B., Schinzel A., Plauchu H., Toutain A., Achard F., Munnich A., Maroteaux P. A gene for hereditary multiple exostoses maps to chromosome 19p. Hum. Mol. Genet. 3:1994;717-722.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 717-722
-
-
Le Merrer, M.1
Legeai-Mallet, L.2
Jeannin, P.M.3
Horsthemke, B.4
Schinzel, A.5
Plauchu, H.6
Toutain, A.7
Achard, F.8
Munnich, A.9
Maroteaux, P.10
-
23
-
-
0031106190
-
Genomic organization and promoter structure of the human EXT1 gene
-
Lüdecke H.-J., Ahn J., Lin X., Hill A., Wagner M. J., Schomburg L., Horsthemke B., Wellls D. E. Genomic organization and promoter structure of the human EXT1 gene. Genomics. 40:1997;351-354.
-
(1997)
Genomics
, vol.40
, pp. 351-354
-
-
Lüdecke, H.-J.1
Ahn, J.2
Lin, X.3
Hill, A.4
Wagner, M.J.5
Schomburg, L.6
Horsthemke, B.7
Wellls, D.E.8
-
24
-
-
0028046406
-
Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors
-
Mathew H., Murty V. V. V. S., Bosl G. J., Chaganti R. S. K. Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors. Cancer Res. 54:1994;6265-6269.
-
(1994)
Cancer Res.
, vol.54
, pp. 6265-6269
-
-
Mathew, H.1
Murty, V.V.V.S.2
Bosl, G.J.3
Chaganti, R.S.K.4
-
25
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki Y., Swensen J., Shattuck-Eidens D., Futreal P. A., Harschman K., Tavtigian S., Liu Q., Chochran C., Bennet L. M., Ding W., Bell R., Rosenthal J., Hussey C., Tran T., McClure M., Frye C., Hattier T., Phelps R., Haugen-Trano A., Katcher H., Yakumo K., Gholami Z., Shaffer D., Stone S., Bayer S., Wray C., Bogden R., Dayananth P., Ward J., Tonin P., Narod S., Bristow P. K., Norris F. H., Helvering L., Morrison P., Rosteck P., Lai M., Barret J. C., Lewis C., Neuhausen S., Cannon-Albright L., Goldgar D., Wiseman R., Kamb A., Skolnick M. H. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science. 266:1994;66-71.
-
(1994)
Science
, vol.266
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
Futreal, P.A.4
Harschman, K.5
Tavtigian, S.6
Liu, Q.7
Chochran, C.8
Bennet, L.M.9
Ding, W.10
Bell, R.11
Rosenthal, J.12
Hussey, C.13
Tran, T.14
McClure, M.15
Frye, C.16
Hattier, T.17
Phelps, R.18
Haugen-Trano, A.19
Katcher, H.20
Yakumo, K.21
Gholami, Z.22
Shaffer, D.23
Stone, S.24
Bayer, S.25
Wray, C.26
Bogden, R.27
Dayananth, P.28
Ward, J.29
Tonin, P.30
Narod, S.31
Bristow, P.K.32
Norris, F.H.33
Helvering, L.34
Morrison, P.35
Rosteck, P.36
Lai, M.37
Barret, J.C.38
Lewis, C.39
Neuhausen, S.40
Cannon-Albright, L.41
Goldgar, D.42
Wiseman, R.43
Kamb, A.44
Skolnick, M.H.45
more..
-
26
-
-
0028918250
-
Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer
-
Nagai H., Negrini M., Carter S. L., Gillum D. R., Rosenberg A. L., Schwartz G. F., Croce C. M. Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer. Cancer Res. 55:1995;1752-1757.
-
(1995)
Cancer Res.
, vol.55
, pp. 1752-1757
-
-
Nagai, H.1
Negrini, M.2
Carter, S.L.3
Gillum, D.R.4
Rosenberg, A.L.5
Schwartz, G.F.6
Croce, C.M.7
-
27
-
-
0028916693
-
Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosome 8 and 11
-
Raskind W. H., Conrad E. U., Chansky H., Matsushita M. Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosome 8 and 11. Am. J. Hum. Genet. 56:1995;1132-1139.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 1132-1139
-
-
Raskind, W.H.1
Conrad, E.U.2
Chansky, H.3
Matsushita, M.4
-
29
-
-
0031045260
-
Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: Linkage in German breast cancer families
-
Seitz S., Rohde K., Bender E., Nothnagel A., Kölbe K., Schlag P. M., Scherneck S. Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: Linkage in German breast cancer families. Oncogene. 14:1997;741-743.
-
(1997)
Oncogene
, vol.14
, pp. 741-743
-
-
Seitz, S.1
Rohde, K.2
Bender, E.3
Nothnagel, A.4
Kölbe, K.5
Schlag, P.M.6
Scherneck, S.7
-
30
-
-
0030933762
-
Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lackingBrca2
-
Sharan S. K., Morimatsu M., Albrecht U., Lim D. S., Regel E., Dinh C., Sands S., Eichele G., Hasty P., Bradley A. Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lackingBrca2. Nature. 386:1997;804-810.
-
(1997)
Nature
, vol.386
, pp. 804-810
-
-
Sharan, S.K.1
Morimatsu, M.2
Albrecht, U.3
Lim, D.S.4
Regel, E.5
Dinh, C.6
Sands, S.7
Eichele, G.8
Hasty, P.9
Bradley, A.10
-
31
-
-
0001524698
-
Hereditary multiple exostoses
-
Solomon L. Hereditary multiple exostoses. Am. J. Hum. Genet. 16:1964;351-363.
-
(1964)
Am. J. Hum. Genet.
, vol.16
, pp. 351-363
-
-
Solomon, L.1
-
32
-
-
0029764629
-
The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes
-
Stickens D., Clines G., Burbee D., Ramos P., Thomas S., Hogue D., Hecht J. T., Lovett M., Evans G. A. The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes. Nature Genet. 14:1996;25-32.
-
(1996)
Nature Genet.
, vol.14
, pp. 25-32
-
-
Stickens, D.1
Clines, G.2
Burbee, D.3
Ramos, P.4
Thomas, S.5
Hogue, D.6
Hecht, J.T.7
Lovett, M.8
Evans, G.A.9
-
33
-
-
0027853058
-
Recurrent deletions of specific chromosomal sites in 1p, 3p, 6q and 9p in human malignant mesothelioma
-
Taguchi T., Jhanwar S. C., Siegfried J. M., Keller S. M., Testa J. R. Recurrent deletions of specific chromosomal sites in 1p, 3p, 6q and 9p in human malignant mesothelioma. Cancer Res. 53:1993;4349-4355.
-
(1993)
Cancer Res.
, vol.53
, pp. 4349-4355
-
-
Taguchi, T.1
Jhanwar, S.C.2
Siegfried, J.M.3
Keller, S.M.4
Testa, J.R.5
-
34
-
-
0027484115
-
High-resolution fluorescence mapping of 46 markers on the short arm of chromosome 1
-
Van Roy N., Laureys G., Versteeg R., Opdenakker G., Speleman F. High-resolution fluorescence mapping of 46 markers on the short arm of chromosome 1. Genomics. 18:1993;71-78.
-
(1993)
Genomics
, vol.18
, pp. 71-78
-
-
Van Roy, N.1
Laureys, G.2
Versteeg, R.3
Opdenakker, G.4
Speleman, F.5
-
36
-
-
0031051305
-
Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family
-
Wise C. A., Clines G. A., Massa H., Trask B. J., Lovett M. Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family. Genome Res. 7:1997;10-16.
-
(1997)
Genome Res.
, vol.7
, pp. 10-16
-
-
Wise, C.A.1
Clines, G.A.2
Massa, H.3
Trask, B.J.4
Lovett, M.5
-
37
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
Wooster R., Bignell G., Lancaster J., Swift S., Seal S., Mangion J., Collins N., Gregory S., Gumbs C., Micklem G., Barfoot R., Hamoudi R., Patel S., Rice C., Biggs P., Hashim Y., Smith A., Connor F., Arason A., Gudmundsson J., Ficenec D., Kelsell D., Ford D., Tonin P., Bishop T. D., Spurr N. K., Ponder B. A. J., Eeles R., Peto J., Devilee P., Cornelisse C., Lynch H., Narod S., Lenoir G., Eglisson V., Bjork-Barkadottir R., Easton D. F., Bentley D. R., Futreal P. A., Ashworth A., Stratton M. R. Identification of the breast cancer susceptibility gene BRCA2. Nature. 378:1995;789-792.
-
(1995)
Nature
, vol.378
, pp. 789-792
-
-
Wooster, R.1
Bignell, G.2
Lancaster, J.3
Swift, S.4
Seal, S.5
Mangion, J.6
Collins, N.7
Gregory, S.8
Gumbs, C.9
Micklem, G.10
Barfoot, R.11
Hamoudi, R.12
Patel, S.13
Rice, C.14
Biggs, P.15
Hashim, Y.16
Smith, A.17
Connor, F.18
Arason, A.19
Gudmundsson, J.20
Ficenec, D.21
Kelsell, D.22
Ford, D.23
Tonin, P.24
Bishop, T.D.25
Spurr, N.K.26
Ponder, B.A.J.27
Eeles, R.28
Peto, J.29
Devilee, P.30
Cornelisse, C.31
Lynch, H.32
Narod, S.33
Lenoir, G.34
Eglisson, V.35
Bjork-Barkadottir, R.36
Easton, D.F.37
Bentley, D.R.38
Futreal, P.A.39
Ashworth, A.40
Stratton, M.R.41
more..
-
38
-
-
0028047748
-
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11
-
Wu Y., Heutink P., de Vries B., Sandkuijl L. A., van den Ouweland A. M. W., Niermeijer M. F., Galjaard H., Reyniers E., Willems P. J., Halley D. J. J. Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11. Hum. Mol. Genet. 3:1994;167-171.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 167-171
-
-
Wu, Y.1
Heutink, P.2
De Vries, B.3
Sandkuijl, L.A.4
Van Den Ouweland, A.M.W.5
Niermeijer, M.F.6
Galjaard, H.7
Reyniers, E.8
Willems, P.J.9
Halley, D.J.J.10
-
39
-
-
0029047022
-
Refinement of the multiple exostoses locus (EXT2) to a 3 cM interval on chromosome 11
-
Wuyts W., Ramlakhan S., Van Hul W., Hecht J. T., van den Ouweland A. M. W., Raskind W., Hofstede F. C., Reyniers E., Wells D. E., de Vries B., Conrad E. U., Hill A., Zalatayev D., Weissenbach J., Wagner M. J., Bakker E., Halley D. J. J., Willems P. J. Refinement of the multiple exostoses locus (EXT2) to a 3 cM interval on chromosome 11. Am. J. Hum. Genet. 57:1995;382-387.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 382-387
-
-
Wuyts, W.1
Ramlakhan, S.2
Van Hul, W.3
Hecht, J.T.4
Van Den Ouweland, A.M.W.5
Raskind, W.6
Hofstede, F.C.7
Reyniers, E.8
Wells, D.E.9
De Vries, B.10
Conrad, E.U.11
Hill, A.12
Zalatayev, D.13
Weissenbach, J.14
Wagner, M.J.15
Bakker, E.16
Halley, D.J.J.17
Willems, P.J.18
-
40
-
-
10144253124
-
Positional cloning of a gene involved in hereditary multiple exostoses
-
Wuyts W., Van Hul W., Wauters J., Nemtsova M., Reyniers E., Van Hul E., De Boulle K., de Vries B. B. A., Hendrickx J., Herrygers I., Bossuyt P., Balemans W., Fransen E., Vits L., Coucke P., Nowak N. J., Shows T. B., Mallet L., van den Ouweland A. M. W., McGaughran J., Halley D. J. J., Willems P. J. Positional cloning of a gene involved in hereditary multiple exostoses. Hum. Mol. Genet. 5:1996;1547-1557.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1547-1557
-
-
Wuyts, W.1
Van Hul, W.2
Wauters, J.3
Nemtsova, M.4
Reyniers, E.5
Van Hul, E.6
De Boulle, K.7
De Vries, B.B.A.8
Hendrickx, J.9
Herrygers, I.10
Bossuyt, P.11
Balemans, W.12
Fransen, E.13
Vits, L.14
Coucke, P.15
Nowak, N.J.16
Shows, T.B.17
Mallet, L.18
Van Den Ouweland, A.M.W.19
McGaughran, J.20
Halley, D.J.J.21
Willems, P.J.22
more..
-
41
-
-
85030300522
-
Identification and characterization of a novel member of the EXT gene family
-
Wuyts, W. Van Hul, W. Hendrickx, J. Wauters, J. Speleman, F. De Boulle, K. Bossuyt, P. Van Agtmael, T. Willems, P. J. Identification and characterization of a novel member of the EXT gene family, EXTL2.
-
EXTL2
-
-
Wuyts, W.1
Van Hul, W.2
Hendrickx, J.3
Wauters, J.4
Speleman, F.5
De Boulle, K.6
Bossuyt, P.7
Van Agtmael, T.8
Willems, P.J.9
-
42
-
-
0028111570
-
Frequent genetic alterations at distal regions of chromosome 1p in human hepatocellular carcinomas
-
Yeh S. H., Chen P. J., Chen H. L., Lai M. Y., Wang C. C., Chen D. S. Frequent genetic alterations at distal regions of chromosome 1p in human hepatocellular carcinomas. Cancer Res. 54:1994;4188-4192.
-
(1994)
Cancer Res.
, vol.54
, pp. 4188-4192
-
-
Yeh, S.H.1
Chen, P.J.2
Chen, H.L.3
Lai, M.Y.4
Wang, C.C.5
Chen, D.S.6
|