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Results of search for 'su:"Chromosome Fragility"', page 35 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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681.
The effect of 1-beta-D-arabinofuranosyl-cytosine on the expression of the common fragile site at 3p14.
[electronic resource]
by
Li, X Z
Yan, Z A
Zhou, X T
Producer:
19870211
In:
Human genetics
vol. 74
Online resources:
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682.
Synergistic effect of DAPI and thymidylate stress conditions on the induction of common fragile sites.
[electronic resource]
by
Rocchi, A
Pelliccia, F
Producer:
19881222
In:
Cytogenetics and cell genetics
vol. 48
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683.
Translocations of chromosome 12. II. A comparison of the distribution of sites of spontaneous and induced breakages.
[electronic resource]
by
Ford, J H
Producer:
19820412
In:
Human genetics
vol. 58
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684.
Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences.
[electronic resource]
by
Rossi, E
Floridia, G
Casali, M
Danesino, C
Chiumello, G
Bernardi, F
Magnani, I
Papi, L
Mura, M
Zuffardi, O
Producer:
19940304
In:
Journal of medical genetics
vol. 30
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685.
Physical localisation of the breakpoints of a constitutional translocation t(5;6)(q21;q21) in a child with bilateral Wilms' tumour.
[electronic resource]
by
Hoban, P R
Cowen, R L
Mitchell, E L
Evans, D G
Kelly, M
Howard, P J
Heighway, J
Producer:
19970729
In:
Journal of medical genetics
vol. 34
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686.
[Medical pathology due to trinucleotide repeats].
[electronic resource]
by
Arenas-Aranda, D
Peñaloza, R
Salamanca-Gómez, F
Producer:
19990503
In:
Gaceta medica de Mexico
vol. 135
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687.
The clinical significance of fragile sites on human chromosomes.
[electronic resource]
by
Sutherland, G R
Baker, E
Producer:
20010215
In:
Clinical genetics
vol. 58
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688.
Fragile sites and neuroblastoma: fragile site at 1p13.1 and other points on lymphocyte chromosomes from patients and family members.
[electronic resource]
by
Rudolph, B
Harbott, J
Lampert, F
Producer:
19880408
In:
Cancer genetics and cytogenetics
vol. 31
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689.
Sister chromatid exchange induced by X-irradiation of retinoblastoma lymphocytes.
[electronic resource]
by
Abramovsky-Kaplan, I
Jones, I S
Producer:
19840718
In:
Investigative ophthalmology & visual science
vol. 25
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690.
Prenatal diagnosis of Martin-Bell syndrome associated with fragile site at Xq27-28.
[electronic resource]
by
Webb, T
Butler, D
Insley, J
Weaver, J B
Green, S
Rodeck, C
Producer:
19820222
In:
Lancet (London, England)
vol. 2
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691.
Possible involvement of unstable sites on chromosomes 7 and 14 in human cancer.
[electronic resource]
by
Scheres, J M
Hustinx, T W
Trent, J M
Producer:
19860123
In:
Cancer genetics and cytogenetics
vol. 19
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692.
Marker X syndrome in an oriental family with probable transmission by a normal male.
[electronic resource]
by
Rhoads, F A
Oglesby, A C
Mayer, M
Jacobs, P A
Producer:
19820924
In:
American journal of medical genetics
vol. 12
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693.
A new autosomal recessive anomaly mimicking Fanconi's anaemia phenotype.
[electronic resource]
by
Milner, R D
Khallouf, K A
Gibson, R
Hajianpour, A
Mathew, C G
Producer:
19930316
In:
Archives of disease in childhood
vol. 68
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694.
Metaphase fragility of the human RNU1 and RNU2 loci is induced by actinomycin D through a p53-dependent pathway.
[electronic resource]
by
Yu, A
Bailey, A D
Weiner, A M
Producer:
19980512
In:
Human molecular genetics
vol. 7
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695.
Identifying chromosomal fragile sites from a hierarchical-clustering point of view.
[electronic resource]
by
Hou, C D
Chiang, J
Tai, J J
Producer:
20011204
In:
Biometrics
vol. 57
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696.
New classes of common fragile sites induced by 5-azacytidine and bromodeoxyuridine.
[electronic resource]
by
Sutherland, G R
Parslow, M I
Baker, E
Producer:
19850514
In:
Human genetics
vol. 69
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697.
Folic acid sensitive fragile sites are not limited to the human karyotype. Demonstration of nonrandom gaps and breaks in the Persian vole Ellobius lutescens Th. inducible by methotrexate, fluorodeoxyuridine, and aphidicolin.
[electronic resource]
by
Djalali, M
Barbi, G
Steinbach, P
Producer:
19850801
In:
Human genetics
vol. 70
Online resources:
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698.
The effect of caffeine on fragile X expression.
[electronic resource]
by
Abruzzo, M A
Pettay, D
Mayer, M
Jacobs, P A
Producer:
19860709
In:
Human genetics
vol. 73
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699.
Synergism between aphidicolin and adenoviruses in the induction of breaks at fragile sites on human chromosomes.
[electronic resource]
by
Caporossi, D
Bacchetti, S
Nicoletti, B
Producer:
19910813
In:
Cancer genetics and cytogenetics
vol. 54
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700.
Frequency of fragile X chromosomes, fra(X), in lymphocytes in relation to blood storage time and culture techniques.
[electronic resource]
by
Fonatsch, C
Schwinger, E
Producer:
19830909
In:
Human genetics
vol. 64
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