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Results of search for 'su:"Chromosome Fragility"', page 44 of 71
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Authors
Baker, E
Brown, W T
Caporossi, D
Croce, C M
Davies, K E
Glover, T W
Halbrecht, I
Hecht, B K
Hecht, F
Hori, T
Huebner, K
Jenkins, E C
Nicoletti, B
Richards, R I
Shabtai, F
Smith, D I
Sutherland, G R
Takahashi, E
Tedeschi, B
Vernole, P
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Topics
Adult
Animals
Cells, Cultured
Chromosome Aberrations
Chromosome Banding
Chromosome Fragile Sites
Chromosome Fragility
Chromosome Mapping
Female
Fragile X Syndrome
Humans
Karyotyping
Lymphocytes
Male
Middle Aged
X Chromosome
drug effects
genetics
pharmacology
ultrastructure
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Results
861.
Genetic recombination in human melanoma and astrocytoma cell lines involves oncogenes and growth factor genes.
[electronic resource]
by
Lakshmi, M S
Sherbet, G V
Producer:
19900206
In:
Clinical & experimental metastasis
vol. 8
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862.
Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.
[electronic resource]
by
Voelckel, M A
Philip, N
Piquet, C
Pellissier, M C
Oberlé, I
Birg, F
Mattei, M G
Mattei, J F
Producer:
19890512
In:
Human genetics
vol. 81
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863.
Variability in expression of common fragile sites: in search of a new criterion.
[electronic resource]
by
Jordan, D K
Burns, T L
Divelbiss, J E
Woolson, R F
Patil, S R
Producer:
19901205
In:
Human genetics
vol. 85
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864.
Autism and the fragile X syndrome.
[electronic resource]
by
Fisch, G S
Cohen, I L
Wolf, E G
Brown, W T
Jenkins, E C
Gross, A
Producer:
19860205
In:
The American journal of psychiatry
vol. 143
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865.
DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes.
[electronic resource]
by
Glover, T W
Berger, C
Coyle, J
Echo, B
Producer:
19840919
In:
Human genetics
vol. 67
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866.
The expression of common fragile sites in peripheral blood lymphocytes of breast and colorectal cancer patients with aphidicolin.
[electronic resource]
by
Balci, A
Ekmekci, A
Cetin, R
Producer:
20000621
In:
The Tohoku journal of experimental medicine
vol. 189
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867.
Assignment of FRA1H common fragile site to human chromosome band 1q42.1 proximal to the nuclear NAD+ ADP-ribosyltransferase gene (ADPRT) and to the main 5S rRNA gene locus.
[electronic resource]
by
Pelliccia, F
Limongi, M Z
Gaddini, L
Rocchi, A
Producer:
19981106
In:
Cytogenetics and cell genetics
vol. 82
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868.
Recurrent chromosomal rearrangements involving breakpoints 3p21 and 19q13 in Chinese IgD multiple myeloma detected by G-banding and multicolor spectral karyotyping: a review of IgD karyotype literature.
[electronic resource]
by
Ng, M H
Wong, N
Tsang, K S
Cheng, S H
Chung, Y F
Lo, K W
Producer:
20011018
In:
Human pathology
vol. 32
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869.
Chromosomal defects in 34 male homosexuals, half of them with HIV antibodies.
[electronic resource]
by
Castro-Volio, Isabel
Valle-Bourrette, Luisa
Producer:
20021220
In:
Revista de biologia tropical
vol. 50
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870.
Replication dynamics at common fragile site FRA6E.
[electronic resource]
by
Palumbo, Elisa
Matricardi, Laura
Tosoni, Elena
Bensimon, Aaron
Russo, Antonella
Producer:
20110222
In:
Chromosoma
vol. 119
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871.
Autosomal folate sensitive fragile sites in normal and mentally retarded individuals in Greece.
[electronic resource]
by
Mavrou, A
Syrrou, M
Tsenghi, C
Metaxotou, C
Producer:
19910521
In:
American journal of medical genetics
vol. 38
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872.
Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.
[electronic resource]
by
Mattei, M G
Baeteman, M A
Heilig, R
Oberlé, I
Davies, K
Mandel, J L
Mattei, J F
Producer:
19850530
In:
Human genetics
vol. 69
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873.
Major histocompatibility complex, t-complex, and leukemia.
[electronic resource]
by
Dorak, M T
Burnett, A K
Producer:
19920730
In:
Cancer causes & control : CCC
vol. 3
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874.
Clustering of C2-H2 zinc finger motif sequences within telomeric and fragile site regions of human chromosomes.
[electronic resource]
by
Lichter, P
Bray, P
Ried, T
Dawid, I B
Ward, D C
Producer:
19920922
In:
Genomics
vol. 13
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875.
Aphidicolin-induced FRA3B breakpoints cluster in two distinct regions.
[electronic resource]
by
Wang, L
Paradee, W
Mullins, C
Shridhar, R
Rosati, R
Wilke, C M
Glover, T W
Smith, D I
Producer:
19970701
In:
Genomics
vol. 41
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876.
Characterization of the common fragile site FRA9E and its potential role in ovarian cancer.
[electronic resource]
by
Callahan, Gwen
Denison, Stacy R
Phillips, Leslie A
Shridhar, Viji
Smith, David I
Producer:
20030212
In:
Oncogene
vol. 22
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877.
Co-localisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome: evidence for a common mechanism of chromosome breakage.
[electronic resource]
by
Jones, C
Müllenbach, R
Grossfeld, P
Auer, R
Favier, R
Chien, K
James, M
Tunnacliffe, A
Cotter, F
Producer:
20000623
In:
Human molecular genetics
vol. 9
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878.
Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomalies.
[electronic resource]
by
Lavanchy, L
Munier, F L
Cousin, P
Gaide, A C
Thonney, F
Schorderet, D F
Producer:
20010621
In:
Ophthalmic genetics
vol. 22
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879.
Trinucleotide repeats and other microsatellites in yeasts.
[electronic resource]
by
Richard, G F
Hennequin, C
Thierry, A
Dujon, B
Producer:
20000301
In:
Research in microbiology
vol. 150
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880.
Loss of Ubr2, an E3 ubiquitin ligase, leads to chromosome fragility and impaired homologous recombinational repair.
[electronic resource]
by
Ouyang, Yan
Kwon, Yong Tae
An, Jee Young
Eller, Danny
Tsai, Shih-Chang
Diaz-Perez, Silvia
Troke, Joshua J
Teitell, Michael A
Marahrens, York
Producer:
20060705
In:
Mutation research
vol. 596
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