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Results of search for 'su:"Chromosome Fragility"', page 29 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
561.
Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis.
[electronic resource]
by
Wang, H
McLaughlin, M
Thompson, C
Hunter, A G
Producer:
19930730
In:
American journal of medical genetics
vol. 46
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562.
No cytogenetic evidence for involvement of gene(s) at 2p16 in sporadic cardiac myxomas: cytogenetic changes in ten sporadic cardiac myxomas.
[electronic resource]
by
Dijkhuizen, T
de Jong, B
Meuzelaar, J J
Molenaar, W M
van den Berg, E
Producer:
20010621
In:
Cancer genetics and cytogenetics
vol. 126
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563.
Induction of fragility at the human RNU2 locus by cytosine arabinoside is dependent upon a transcriptionally competent U2 small nuclear RNA gene and the expression of p53.
[electronic resource]
by
MacArthur, H L
Agarwal, M L
Bacchetti, S
Producer:
19980723
In:
Somatic cell and molecular genetics
vol. 23
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564.
When smoke gets in your genes.
[electronic resource]
by
Sozzi, G
Pierotti, M A
Producer:
19981028
In:
Nature medicine
vol. 4
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565.
A new folate sensitive fragile site at 1p21.3.
[electronic resource]
by
Baker, E
Sutherland, G R
Producer:
19910906
In:
Journal of medical genetics
vol. 28
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566.
Fragile 3p14 in patients with von Hippel-Lindau syndrome compared to controls.
[electronic resource]
by
Webb, T
Heath, D
Producer:
19920131
In:
Cancer genetics and cytogenetics
vol. 56
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567.
[Molecular construction of Philadelphia chromosome and its relation to the clinical features].
[electronic resource]
by
Kamada, N
Tanaka, K
Asou, H
Producer:
19910722
In:
Gan to kagaku ryoho. Cancer & chemotherapy
vol. 18
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568.
Fragile X chromosome in institutionalized male adults with mental retardation.
[electronic resource]
by
Aoi, T
Takashima, H
Takada, T
Okada, T
Producer:
19890622
In:
The Keio journal of medicine
vol. 38
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569.
First intron and M-bcr breakpoints are restricted to the lymphoid lineage in Philadelphia positive acute lymphoblastic leukemia.
[electronic resource]
by
Craig, J M
Hawkins, J M
Yamada, T
Ganeshaguru, K
Mehta, A B
Secker-Walker, L M
Producer:
19901119
In:
Leukemia
vol. 4
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570.
Common fragile sites induced by folate deprivation, BrdU and aphidicolin: their frequency and distribution in Japanese individuals.
[electronic resource]
by
Kuwano, A
Sugio, Y
Murano, I
Kajii, T
Producer:
19890207
In:
Jinrui idengaku zasshi. The Japanese journal of human genetics
vol. 33
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571.
Fragile sites are targets of diverse mutagens and carcinogens.
[electronic resource]
by
Yunis, J J
Soreng, A L
Bowe, A E
Producer:
19880330
In:
Oncogene
vol. 1
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572.
Role of chromosome aberrations in recurrent abortion: a study of 269 balanced translocations.
[electronic resource]
by
Campana, M
Serra, A
Neri, G
Producer:
19860627
In:
American journal of medical genetics
vol. 24
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573.
A marker X chromosome associated with nonspecific male mental retardation. The first South African cases.
[electronic resource]
by
Venter, P A
Gericke, G S
Dawson, B
Op't Hof, J
Producer:
19820128
In:
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde
vol. 60
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574.
Expression in lymphocyte and fibroblast culture of the fragile X chromosome: a new technical approach.
[electronic resource]
by
Mattei, M G
Mattei, J F
Vidal, I
Giraud, F
Producer:
19820422
In:
Human genetics
vol. 59
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575.
Variant Ph translocations in chronic myeloid leukemia.
[electronic resource]
by
Heim, S
Billström, R
Kristoffersson, U
Mandahl, N
Strömbeck, B
Mitelman, F
Producer:
19851206
In:
Cancer genetics and cytogenetics
vol. 18
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576.
Human chromosomes: evaluation of processing techniques for scanning electron microscopy.
[electronic resource]
by
Sanchez-Sweatman, O H
de Harven, E P
Dubé, I D
Producer:
19930728
In:
Scanning microscopy
vol. 7
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577.
DNA structures at chromosomal translocation sites.
[electronic resource]
by
Raghavan, Sathees C
Lieber, Michael R
Producer:
20060623
In:
BioEssays : news and reviews in molecular, cellular and developmental biology
vol. 28
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578.
Chromosome fragility: molecular mechanisms and cellular consequences.
[electronic resource]
by
Freudenreich, Catherine H
Producer:
20070810
In:
Frontiers in bioscience : a journal and virtual library
vol. 12
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579.
Monosomy, trisomy, fragile sites, and rearrangements of chromosome no. 1 in a mentally retarded male with multiple congenital anomalies.
[electronic resource]
by
Neu, R L
Kousseff, B G
Madan, S
Essig, Y P
Miller, K
Tedesco, T A
Producer:
19880527
In:
Clinical genetics
vol. 33
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580.
The fragile site (17)(p12): induction by AT-specific DNA-ligands and population cytogenetics.
[electronic resource]
by
Schmid, M
Feichtinger, W
Deubelbeiss, C
Weller, E
Producer:
19871117
In:
Human genetics
vol. 77
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