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H. Christiansen, F. Lampert (1988)
Tumour karyotype discriminates between good and bad prognostic outcome in neuroblastoma.British Journal of Cancer, 57
Yuesheng Jin, K. Higashi, N. Mandahl, S. Heim, J. Wennerberg, A. Biörklund, M. Dictor, F. Mitelman (1990)
Frequent rearrangement of chromosomal bands 1p22 and 11q13 in squamous cell carcinomas of the head and neckGenes, 2
R. Mead, J. Cowell (1995)
Molecular characterization of a (1;10)(p22;q21) constitutional translocation from a patient with neuroblastoma.Cancer genetics and cytogenetics, 81 2
F. Cotter, G. Hampton, S. Nasipuri, W. Bodmer, B. Young (1990)
Rapid isolation of human chromosome-specific DNA probes from a somatic cell hybrid.Genomics, 7 2
Ivan Bièche, M. Champème, F. Matifas, C. Cropp, Robert Callahan, R. Lidereau (1993)
Two distinct regions involved in 1p deletion in human primary breast cancer.Cancer research, 53 9
M. Engelstein, T. Hudson, Joan Lane, Matthias Lee, B. Leverone, G. Landes, Elena Peltonen, J. Weber, N. Dracopoli (1993)
A PCR-based linkage map of human chromosome 1.Genomics, 15 2
J. Hunt, A. Tereba (1990)
Molecular evaluation of abnormalities of the short arm of chromosome I in neuroblastomaGenes, 2
T. Mohandas (1994)
A somatic cell hybrid mapping panel for human chromosome 1, 67
A. Collins, B. Keats, N. Dracopoli, D. Shields, N. Morton (1992)
Integration of gene maps: chromosome 1.Proceedings of the National Academy of Sciences of the United States of America, 89
(1992)
Detection of heterozygous mutations in the RB 1 gene in retinoblastoma patients using single strand conformation polymorphism ( SSCP ) . analysis and PCR sequencing
R. Vanni, P. Cin, H. Berghe (1990)
Is the chromosome band 1p36 another hot‐spot for rearrangements in uterine leiomyoma?Genes, 2
M. Anderson, C. Fasching, E. Stanbridge, G. Casey (1994)
Evidence that wild‐type TP53, and not genes on either chromosome 1 or 11, controls the tumorigenic phenotype of the human fibrosarcoma HT1080Genes, 9
W. Cavenee, W. Cavenee, T. Dryja, R. Phillips, W. Benedict, R. Godbout, B. Gallie, A. Murphree, L. Strong, Raymond White (1983)
Expression of recessive alleles by chromosomal mechanisms in retinoblastomaNature, 305
L. Hawthorn, J. Cowell (1995)
Integration of the physical and genetic linkage map for human chromosome 13.Genomics, 27 3
L. Hawthorn, R. Chapman, D. Oscier, J. Cowell (1993)
The consistent 13q14 translocation breakpoint seen in chronic B-cell leukaemia (BCLL) involves deletion of the D13S25 locus which lies distal to the retinoblastoma predisposition gene.Oncogene, 8 6
M. Adams, M. Dubnick, A. Kerlavage, R. Moreno, J. Kelley, T. Utterback, James Nagle, C. Fields, J. Venter (1992)
Sequence identification of 2,375 human brain genesNature, 355
M. Polymeropoulos, Hong Xiao, J. Sikela, M. Adams, J. Venter, C. Merril (1993)
Chromosomal distribution of 320 genes from a brain cDNA libraryNature Genetics, 4
V. Solís, J. Pritchard, J. Cowell (1988)
Cytogenetic changes in Wilms' tumors.Cancer genetics and cytogenetics, 34 2
A. Michalski, J. Cowell (1993)
Assignment of four sequence-tagged sites to three subregions of 13q12 using a somatic cell hybrid mapping panel.Genomics, 18 1
B. Horsthemke (1992)
Genetics and cytogenetics of retinoblastoma.Cancer genetics and cytogenetics, 63 1
P. Devilee, Margreethe Vhet, A. Bardoel, Tim Kievits, N. Kuipers-Dijkshoorn, Peter Pearson, C. Cornelisse, Pathology ¡n, K-D (1991)
Frequent somatic imbalance of marker alleles for chromosome 1 in human primary breast carcinoma.Cancer research, 51 3
K. Buetow, D. Nishimura, Y. Nakamura, O. Jiang, J. Murray (1990)
A detailed multipoint gene map of chromosome 1q.Genomics, 8 1
N. Roy, G. Laureys, R. Versteeg, G. Opdenakker, F. Speleman (1993)
High-resolution fluorescence mapping of 46 DNA markers to the short arm of human chromosome 1.Genomics, 18 1
J. Squire, B. L. Gallie, R. A. Phillips (1985)
A detailed analysis of chromosomal changes in heritable and non‐heritable retinoblastoma, 70
G. Rouleau, A. Bazanowski, J. Gusella, J. Haines (1990)
A genetic map of chromosome 1: comparison of different data sets and linkage programs.Genomics, 7 3
N. Dracopoli, Paul HARNETTt, S. Bales, B. Stanger, Margaret TUCKERt, D. Housman, Richard KEFFORDt (1989)
Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression.Proceedings of the National Academy of Sciences of the United States of America, 86 12
V. Solis, J. Pritchard, J. K. Cowell (1988)
Cytogenetics of Wilms' tumours, 34
V. Brito‐Babapulle, N. Atkin (1981)
Break points in chromosome #1 abnormalities of 218 human neoplasms.Cancer genetics and cytogenetics, 4 3
A. Michalski, F. Cotter, J. Cowell (1992)
Isolation of chromosome-specific DNA sequences from an Alu polymerase chain reaction library to define the breakpoint in a patient with a constitutional translocation t(1;13) (q22;q12) and ganglioneuroblastoma.Oncogene, 7 8
V. Cryns, Sunmi Yi, H. Tahara, R. Gaz, A. Arnold (1995)
Frequent loss of chromosome arm Ip DNA in parathyroid adenomasGenes, 13
D. Simon, B. Knowles, A. Weith (1991)
Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatomas.Oncogene, 6 5
C. Cole, P. Goodfellow, M. Bobrow, D. Bentley (1991)
Generation of novel sequence tagged sites (STSs) from discrete chromosomal regions using Alu-PCR.Genomics, 10 3
L. Hawthorn, T. Roberts, E. Verlind, R. Kooy, J. Cowell (1995)
A yeast artificial chromosome contig that spans the RB1-D13S31 interval on human chromosome 13 and encompasses the frequently deleted region in B-cell chronic lymphocytic leukemia.Genomics, 30 3
G. Gyapay, J. Morissette, A. Vignal, C. Dib, C. Fizames, P. Millasseau, S. Marc, G. Bernardi, M. Lathrop, J. Weissenbach (1994)
The 1993–94 Généthon human genetic linkage mapNature Genetics, 7
R. Slater, M. Mannens (1992)
Cytogenetics and molecular genetics of Wilms' tumor of childhood.Cancer genetics and cytogenetics, 61 2
S. Lawrence, A. Collins, B. Keats, M. Hultén, N. Morton (1992)
Integration of gene maps: chromosome 21.Proceedings of the National Academy of Sciences of the United States of America, 90 15
Ilona Leister, A. Weith, S. Brüderlein, C. Cziepluch, D. Kangwanpong, Peter Schlag, M. Schwab (1990)
Human colorectal cancer: high frequency of deletions at chromosome 1p35.Cancer research, 50 22
A somatic cell hybrid mapping panel has been constructed which allows subdivision of human chromosome 1 into 8 distinct subregions. All of the hybrids carry copies of chromosome 1 with specific deletions and the position of the breakpoints has been determined relative to the location of microsatellite markers in the genetic linkage map produced by Genethon. The majority of the breakpoints can be positioned between adjacent loci on the map. The usefulness of this hybrid panel for physical mapping has been demonstrated by the regional assignment of 6 novel STS markers made from Alu‐PCR clones generated from a hybrid which contains the short arm of chromosome 1.
Annals of Human Genetics – Wiley
Published: Jan 1, 1996
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