-
1
-
-
0003095801
-
Nucleotide excision repair syndromes: Xeroderma pigmentosum. Cockayne syndrome and trichothiodystrophy
-
C. R. Scriver, A. L. Beaudet, W. S. Sly, and D. Vall (eds.), New York: McGraw-Hill, in press
-
Bootsma, D., Cleaver, J. E., Kraemer, K. H., and Hoeijmakers, J. H. J. Nucleotide excision repair syndromes: xeroderma pigmentosum. Cockayne syndrome and trichothiodystrophy. In: C. R. Scriver, A. L. Beaudet, W. S. Sly, and D. Vall (eds.), The Metabolic Basis of Inherited Disease, Ed. 8. New York: McGraw-Hill, in press, 1998.
-
(1998)
The Metabolic Basis of Inherited Disease, Ed. 8
-
-
Bootsma, D.1
Cleaver, J.E.2
Kraemer, K.H.3
Hoeijmakers, J.H.J.4
-
2
-
-
0026508774
-
Cockayne syndrome: Review of 140 cases
-
Nance, M. A., and Berry, S. A. Cockayne syndrome: review of 140 cases. Am. J. Med. Genet., 42: 68-84, 1992.
-
(1992)
Am. J. Med. Genet.
, vol.42
, pp. 68-84
-
-
Nance, M.A.1
Berry, S.A.2
-
3
-
-
0025276699
-
Trichothiodystrophy: Review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias
-
Itin, P. H., and Pittelkow, M. R. Trichothiodystrophy: review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias. J. Am. Acad. Dermatol., 22: 705-717, 1990.
-
(1990)
J. Am. Acad. Dermatol.
, vol.22
, pp. 705-717
-
-
Itin, P.H.1
Pittelkow, M.R.2
-
4
-
-
0027262205
-
Genetic heterogeneity of the excision repair defect associated with trichothiodystrophy
-
Lond
-
Stefanini, M., Lagomarsini, P., Gilliani, S., Nardo, T., Botta, E., Peserico, A., Kleyer, W. J. Lehmann, A. R., and Sarasin, A. Genetic heterogeneity of the excision repair defect associated with trichothiodystrophy. Carcinogenesis (Lond.), 14: 1101-1105, 1993.
-
(1993)
Carcinogenesis
, vol.14
, pp. 1101-1105
-
-
Stefanini, M.1
Lagomarsini, P.2
Gilliani, S.3
Nardo, T.4
Botta, E.5
Peserico, A.6
Kleyer, W.J.7
Lehmann, A.R.8
Sarasin, A.9
-
5
-
-
0022868911
-
Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity
-
Stefanini, M., Lagomarsini, P., Arlett, C. F., Marinoni, S., Borrone, C., Crovato, F., Trevisan, G., Cordone, G., and Nuzzo, F. Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity. Am. J. Hum. Genet., 74: 107-112, 1986.
-
(1986)
Am. J. Hum. Genet.
, vol.74
, pp. 107-112
-
-
Stefanini, M.1
Lagomarsini, P.2
Arlett, C.F.3
Marinoni, S.4
Borrone, C.5
Crovato, F.6
Trevisan, G.7
Cordone, G.8
Nuzzo, F.9
-
6
-
-
0028362248
-
The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor
-
Schaeffer, L., Moncollin, V., Roy, R., Staub, A., Mezzina, M., Sarasin, A., Weeda, G., Hoeijmakers, J. H. J., and Egly, J-M. The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor. EMBO J., 13: 2388-2392, 1994.
-
(1994)
EMBO J.
, vol.13
, pp. 2388-2392
-
-
Schaeffer, L.1
Moncollin, V.2
Roy, R.3
Staub, A.4
Mezzina, M.5
Sarasin, A.6
Weeda, G.7
Hoeijmakers, J.H.J.8
Egly, J.-M.9
-
7
-
-
0028673969
-
Three unusual repair deficiencies associated with transcription factor BTF2 (TFIIH): Evidence for the existence of a transcription syndrome
-
Vermeulen, W., van Vuuren, A. J., Chipoulet, M., Schaeffer, L., Appeldoorn, E., Weeda, G., Jaspers, N. G. J., Priestley, A., Arlett, C. F., Lehmann, A. R., Stefanini, M., Mezzina, M., Sarasin, A., Bootsma, D., Egly, J-M., and Hoeijmakers, J. H. J. Three unusual repair deficiencies associated with transcription factor BTF2 (TFIIH): evidence for the existence of a transcription syndrome. Cold Spring Harb. Symp. Quant. Biol., 59: 317-329, 1994.
-
(1994)
Cold Spring Harb. Symp. Quant. Biol.
, vol.59
, pp. 317-329
-
-
Vermeulen, W.1
Van Vuuren, A.J.2
Chipoulet, M.3
Schaeffer, L.4
Appeldoorn, E.5
Weeda, G.6
Jaspers, N.G.J.7
Priestley, A.8
Arlett, C.F.9
Lehmann, A.R.10
Stefanini, M.11
Mezzina, M.12
Sarasin, A.13
Bootsma, D.14
Egly, J.-M.15
Hoeijmakers, J.H.J.16
-
9
-
-
0030023261
-
TFIIH: A key component in multiple DNA transactions
-
Hoeijmakers, J. H. J., Egly, J-M., and Vermeulen, W. TFIIH: a key component in multiple DNA transactions. Curr. Opin. Gen. Dev., 6: 26-33, 1996.
-
(1996)
Curr. Opin. Gen. Dev.
, vol.6
, pp. 26-33
-
-
Hoeijmakers, J.H.J.1
Egly, J.-M.2
Vermeulen, W.3
-
10
-
-
0028358988
-
Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy
-
Broughton, B. C., Steingrimsdottir, H., Weber, C. A., and Lehmann, A. R. Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy. Nat. Genet., 7: 189-194, 1994.
-
(1994)
Nat. Genet.
, vol.7
, pp. 189-194
-
-
Broughton, B.C.1
Steingrimsdottir, H.2
Weber, C.A.3
Lehmann, A.R.4
-
11
-
-
0028868125
-
Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome
-
Broughton, B. C., Thompson, A. F., Harcourt, S. A., Vermeulen, W., Hoeijmakers, J. H. J., Botta, E., Stefanini, M., King, M. D., Weber, C. A., Cole, J., Arlett, C. F., and Lehmann, A. R. Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome. Am. J. Hum. Genet., 56: 167-174, 1995.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 167-174
-
-
Broughton, B.C.1
Thompson, A.F.2
Harcourt, S.A.3
Vermeulen, W.4
Hoeijmakers, J.H.J.5
Botta, E.6
Stefanini, M.7
King, M.D.8
Weber, C.A.9
Cole, J.10
Arlett, C.F.11
Lehmann, A.R.12
-
12
-
-
0028832388
-
Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D
-
Takayama, K., Salazar, E. P., Lehmann, A., Stefanini, M., Thompson, L. H., and Weber, C. A. Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D. Cancer Res., 55: 5656-5663, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 5656-5663
-
-
Takayama, K.1
Salazar, E.P.2
Lehmann, A.3
Stefanini, M.4
Thompson, L.H.5
Weber, C.A.6
-
13
-
-
0030051768
-
Defects in the DNA repair and transcription gene ERCC2 (XPD) in trichthiodystrophy
-
Takayama, K., Salazar, E. P., Broughton, B. C., Lehmann, A. R., Sarasin, A., Thompson, L. H., and Weber, C. A. Defects in the DNA repair and transcription gene ERCC2 (XPD) in trichthiodystrophy. Am. J. Hum. Genet., 58: 263-270, 1996.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 263-270
-
-
Takayama, K.1
Salazar, E.P.2
Broughton, B.C.3
Lehmann, A.R.4
Sarasin, A.5
Thompson, L.H.6
Weber, C.A.7
-
14
-
-
16944363270
-
A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy
-
Weeda, G., Eveno, E., Donker, I., Vermeulen, W., Chevallier-Lagente, O., Taïeb, A., Stary, A., Hoeijmakers, J. H. J., Mezzina, M., and Sarasin, A. A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy. Am. J. Hum. Genet., 60: 320-329, 1997.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 320-329
-
-
Weeda, G.1
Eveno, E.2
Donker, I.3
Vermeulen, W.4
Chevallier-Lagente, O.5
Taïeb, A.6
Stary, A.7
Hoeijmakers, J.H.J.8
Mezzina, M.9
Sarasin, A.10
-
15
-
-
0025250069
-
ERCC2: cDNA cloning and molecular characterization of a human nucleotide excision repair gene with high homology to yeast RAD3
-
Weber, C. A., Salazar, E. P., Stewart, S. A., and Thompson, L. H. ERCC2: cDNA cloning and molecular characterization of a human nucleotide excision repair gene with high homology to yeast RAD3. EMBO J., 9: 1437-1447, 1990.
-
(1990)
EMBO J.
, vol.9
, pp. 1437-1447
-
-
Weber, C.A.1
Salazar, E.P.2
Stewart, S.A.3
Thompson, L.H.4
-
16
-
-
0017681196
-
DNA sequencing with chain-terminating inhibitors
-
Sanger, F., Nicklen, S., and Coulson, A. R. DNA sequencing with chain-terminating inhibitors. Proc. Natl. Acad. Sci. USA, 74: 5463-5467, 1977.
-
(1977)
Proc. Natl. Acad. Sci. USA
, vol.74
, pp. 5463-5467
-
-
Sanger, F.1
Nicklen, S.2
Coulson, A.R.3
-
17
-
-
0023646810
-
Site-directed mutagenesis by gene-targeting in mouse embryo-derived stem cells
-
Thomas, K. R., and Capecchi, M. R. Site-directed mutagenesis by gene-targeting in mouse embryo-derived stem cells. Cell, 51: 503-512, 1987.
-
(1987)
Cell
, vol.51
, pp. 503-512
-
-
Thomas, K.R.1
Capecchi, M.R.2
-
18
-
-
0004136246
-
-
Cold Spring Harbor Laboratory, Cold Spring Harbor, NY
-
Sambrook, J., Fritsch, E. F., and Maniatis, T. Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, 1989.
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
19
-
-
0023256867
-
Buffalo rat liver cells produce diffusible activity which inhibits the differentiation of murine carcinoma and embryonic stem cells
-
Smith, A. G., and Hooper, M. Buffalo rat liver cells produce diffusible activity which inhibits the differentiation of murine carcinoma and embryonic stem cells. Dev. Biol., 121: 1-9, 1996.
-
(1996)
Dev. Biol.
, vol.121
, pp. 1-9
-
-
Smith, A.G.1
Hooper, M.2
-
20
-
-
0025739379
-
Simplified mammalian DNA isolation procedure
-
Laird, P. W., Zijderveld, A., Linders, K., Rudnicki, M. A., Jaenisch, R., and Berns, A. Simplified mammalian DNA isolation procedure. Nucleic Acids Res., 19: 4293, 1991.
-
(1991)
Nucleic Acids Res.
, vol.19
, pp. 4293
-
-
Laird, P.W.1
Zijderveld, A.2
Linders, K.3
Rudnicki, M.A.4
Jaenisch, R.5
Berns, A.6
-
21
-
-
0003799070
-
-
Cold Spring Harbor, NY: Cold Spring Harbor Laboratory
-
Hogan, B., Costanti, F., and Lacy, E. Manipulating the Mouse Embryo: A Laboratory Manual. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory, 1986.
-
(1986)
Manipulating the Mouse Embryo: A Laboratory Manual
-
-
Hogan, B.1
Costanti, F.2
Lacy, E.3
-
22
-
-
0025367702
-
Analysis of various mRNA potentially involved in cisplatin resistance of murine leukemia L1210 cell
-
Sheibani, N., and Eastman, A. Analysis of various mRNA potentially involved in cisplatin resistance of murine leukemia L1210 cell. Cancer Lett., 52: 179-185, 1990.
-
(1990)
Cancer Lett.
, vol.52
, pp. 179-185
-
-
Sheibani, N.1
Eastman, A.2
-
23
-
-
0030111466
-
Kinesin proteins: A phylum of motors for microtubule-based motility
-
Moore, J. D., and Endow, S.A. Kinesin proteins: a phylum of motors for microtubule-based motility. BioEssays. 18: 207-219, 1996.
-
(1996)
BioEssays.
, vol.18
, pp. 207-219
-
-
Moore, J.D.1
Endow, S.A.2
-
24
-
-
0030585760
-
Sequence analysis of the ERCC2 gene regions in human, mouse and hamster reveals three linked genes
-
Lamerdin, J. E., Stilwagen, S. A., Ramirez, M. H., Stubbs, L., and Carrano, A. V. Sequence analysis of the ERCC2 gene regions in human, mouse and hamster reveals three linked genes. Genomics, 34: 399-409, 1996.
-
(1996)
Genomics
, vol.34
, pp. 399-409
-
-
Lamerdin, J.E.1
Stilwagen, S.A.2
Ramirez, M.H.3
Stubbs, L.4
Carrano, A.V.5
-
25
-
-
0028958596
-
Characterization of the Xiphophorus fish (Teleostei: Poecilndae) ERCC2/XPD locus
-
Della Coletta, L., Rolig, R. L., Fossey, S., Morizot, D. C., Nairn, R. S., and Walter, R. B. Characterization of the Xiphophorus fish (Teleostei: Poecilndae) ERCC2/XPD locus. Genomics, 26: 70-76, 1995.
-
(1995)
Genomics
, vol.26
, pp. 70-76
-
-
Della Coletta, L.1
Rolig, R.L.2
Fossey, S.3
Morizot, D.C.4
Nairn, R.S.5
Walter, R.B.6
-
26
-
-
0024344173
-
Two related superfamilies of putative helicases involved in replication, recombination, repair and expression of DNA and RNA genomes
-
Gorbalenya, A. E., Koonin, E. V., Donchenko, A. P., and Blinov, V. M. Two related superfamilies of putative helicases involved in replication, recombination, repair and expression of DNA and RNA genomes. Nucleic Acids Res., 17: 4713-4730, 1989.
-
(1989)
Nucleic Acids Res.
, vol.17
, pp. 4713-4730
-
-
Gorbalenya, A.E.1
Koonin, E.V.2
Donchenko, A.P.3
Blinov, V.M.4
-
27
-
-
0028275075
-
Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: Identification of domains essential for the DNA repair function
-
Ma, L., Westbroek, A., Jochemsen, A. G., Weeda, G., Bootsma, D., Hoeijmakers, J. H. J., and van der Eb, A. J. Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: identification of domains essential for the DNA repair function. Mol. Cell. Biol., 14: 4126-4134, 1994.
-
(1994)
Mol. Cell. Biol.
, vol.14
, pp. 4126-4134
-
-
Ma, L.1
Westbroek, A.2
Jochemsen, A.G.3
Weeda, G.4
Bootsma, D.5
Hoeijmakers, J.H.J.6
Van Der Eb, A.J.7
-
28
-
-
0026471044
-
Gene targeting using a mouse HPRT minigene/HPR7-deficient embryonic stem cell system: Inactivation of the mouse ERCC-1 gene
-
Selfridge, J., Pow, A. M., McWhir, J., Magin, T. M., and Melton, D. W. Gene targeting using a mouse HPRT minigene/HPR7-deficient embryonic stem cell system: inactivation of the mouse ERCC-1 gene. Somat. Cell. Mol. Genet., 18: 325-336, 1992.
-
(1992)
Somat. Cell. Mol. Genet.
, vol.18
, pp. 325-336
-
-
Selfridge, J.1
Pow, A.M.2
McWhir, J.3
Magin, T.M.4
Melton, D.W.5
-
29
-
-
0025320883
-
A long-range restriction map of the human chromosome 19q13 region: Close physical linkage between CKMM and the ERCC1 and ERCC2 genes
-
Smeets, H., Bachinski, L., Coerwinkel, M., Schepens, J., Hoeijmakers, J. H. J., van Duin, M., Grzeschik, K. H., Weber, C. A., de Jong, P., Siciliano, M. J., and Wieringa, B. W. A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes. Am. J. Hum. Genet., 46:492-501, 1990.
-
(1990)
Am. J. Hum. Genet.
, vol.46
, pp. 492-501
-
-
Smeets, H.1
Bachinski, L.2
Coerwinkel, M.3
Schepens, J.4
Hoeijmakers, J.H.J.5
Van Duin, M.6
Grzeschik, K.H.7
Weber, C.A.8
De Jong, P.9
Siciliano, M.J.10
Wieringa, B.W.11
-
30
-
-
0024511314
-
Conserved pattern of antisense overlapping transcription in the homologous human ERCC-1 and yeast RADIO DNA repair gene regions
-
van Duin, M., van den Tol, J., Hoeijmakers, J. H. J., Bootsma, D., Rupp, I. P., Reynolds, P., Prakash, L., and Prakash, S. Conserved pattern of antisense overlapping transcription in the homologous human ERCC-1 and yeast RADIO DNA repair gene regions. Mol. Cell. Biol., 9: 1794-1798, 1989.
-
(1989)
Mol. Cell. Biol.
, vol.9
, pp. 1794-1798
-
-
Van Duin, M.1
Van Den Tol, J.2
Hoeijmakers, J.H.J.3
Bootsma, D.4
Rupp, I.P.5
Reynolds, P.6
Prakash, L.7
Prakash, S.8
-
31
-
-
0028140494
-
DNA repair gene RAD 3 of S. cerevisiae is essential for transcription by RNA polymerase II
-
Guzder, S. N., Qiu, H., Sommers, C. H., Sung, P., Prakash, L., and Prakash, S. DNA repair gene RAD 3 of S. cerevisiae is essential for transcription by RNA polymerase II. Nature (Lond.), 367: 91-94, 1994.
-
(1994)
Nature (Lond.)
, vol.367
, pp. 91-94
-
-
Guzder, S.N.1
Qiu, H.2
Sommers, C.H.3
Sung, P.4
Prakash, L.5
Prakash, S.6
-
32
-
-
0025924976
-
DNA-RNA helicase activity of RAD3 protein of Saccharomyces cerevisiae
-
Bailly, V., Sung, P., Prakash, L., and Prakash, S. DNA-RNA helicase activity of RAD3 protein of Saccharomyces cerevisiae. Proc. Natl. Acad Sci. USA, 88: 9712-9716, 1991.
-
(1991)
Proc. Natl. Acad Sci. USA
, vol.88
, pp. 9712-9716
-
-
Bailly, V.1
Sung, P.2
Prakash, L.3
Prakash, S.4
-
33
-
-
0026453401
-
RAD25, a yeast homolog of human xeroderma pigmentosum group B DNA repair gene is essential for viability
-
Park, E., Guzder, S., Koken, M. H., Jaspers-Dekker, I., Weeda, G., Hoeijmakers, J. H. J., Prakash, S., and Prakash, L. RAD25, a yeast homolog of human xeroderma pigmentosum group B DNA repair gene is essential for viability. Proc. Natl. Acad. Sci. USA, 89: 11416-11420, 1992.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 11416-11420
-
-
Park, E.1
Guzder, S.2
Koken, M.H.3
Jaspers-Dekker, I.4
Weeda, G.5
Hoeijmakers, J.H.J.6
Prakash, S.7
Prakash, L.8
-
34
-
-
0027905008
-
DNA repair helicase: A component of BTF2 (TFIIH) basic transcription factor
-
Washington DC
-
Schaeffer, L., Roy, R., Humbert, S., Moncollin, V., Vermeulen, W., Hoeijmakers, J. H. J., Chambon, P., and Egly, J-M. DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor. Science (Washington DC), 260, 58-63, 1993.
-
(1993)
Science
, vol.260
, pp. 58-63
-
-
Schaeffer, L.1
Roy, R.2
Humbert, S.3
Moncollin, V.4
Vermeulen, W.5
Hoeijmakers, J.H.J.6
Chambon, P.7
Egly, J.-M.8
-
35
-
-
0025158110
-
A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome
-
Weeda, G., Van Ham, R. C. A., Vermeulen, W., Bootsma, D., van der Eb, A. J., and Hoeijmakers, J. H. J. A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome. Cell, 62: 777-791, 1990.
-
(1990)
Cell
, vol.62
, pp. 777-791
-
-
Weeda, G.1
Van Ham, R.C.A.2
Vermeulen, W.3
Bootsma, D.4
Van Der Eb, A.J.5
Hoeijmakers, J.H.J.6
-
36
-
-
0020803889
-
A DNA repair gene required for the incision of damaged DNA is essential for viability in Saccharomyces cerevisiae
-
Naumovski, L., and Friedberg, E. C. A DNA repair gene required for the incision of damaged DNA is essential for viability in Saccharomyces cerevisiae. Proc. Natl. Acad. Sci. USA, 80: 4818-4821, 1983.
-
(1983)
Proc. Natl. Acad. Sci. USA
, vol.80
, pp. 4818-4821
-
-
Naumovski, L.1
Friedberg, E.C.2
-
37
-
-
17544402222
-
Isolation and characterization of the RAD3 gene of Saccharomyces cerevisiae and inviability of RAD3 deletion mutants
-
Higgins, D. R., Prakash, S., Reynolds, P., Polakowska, R., Weber, S., and Prakash, L. Isolation and characterization of the RAD3 gene of Saccharomyces cerevisiae and inviability of RAD3 deletion mutants. Proc. Natl. Acad. Sci. USA, 80: 5680-5684, 1983.
-
(1983)
Proc. Natl. Acad. Sci. USA
, vol.80
, pp. 5680-5684
-
-
Higgins, D.R.1
Prakash, S.2
Reynolds, P.3
Polakowska, R.4
Weber, S.5
Prakash, L.6
-
38
-
-
0027073250
-
The genetic program for preimplantation development
-
Kidder, G. M. The genetic program for preimplantation development. Dev. Genet., 13: 319-325, 1992.
-
(1992)
Dev. Genet.
, vol.13
, pp. 319-325
-
-
Kidder, G.M.1
-
39
-
-
0021289440
-
The relationship between cleavage, DNA replication, and gene expression in the mouse 2-cell embryo
-
Bolton, V. N., Oades, P. J., and Johnson, M. H. The relationship between cleavage, DNA replication, and gene expression in the mouse 2-cell embryo. J. Embryol. Exp. Morphol., 79: 139-163, 1984.
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(1984)
J. Embryol. Exp. Morphol.
, vol.79
, pp. 139-163
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Bolton, V.N.1
Oades, P.J.2
Johnson, M.H.3
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