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Results of search for 'su:"Chromosome Fragility"', page 25 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
481.
Chromosomal breaks and sister chromatid exchanges (SCE) in patients with herpetic stomatitis.
[electronic resource]
by
Zervou-Valvi, F
Bazopoulou-Kyrkanidou, E
Angelopoulos, A P
Producer:
19860603
In:
Journal of oral pathology
vol. 15
Online resources:
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482.
Fragile site 1q44 involved in nasopharyngeal carcinoma. A study of a marker chromosome der(1)t(1;3)(q44;p11).
[electronic resource]
by
Xia, J H
Li, L Y
He, X X
Xiao, J Y
Producer:
19881125
In:
Cancer genetics and cytogenetics
vol. 35
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483.
Schizophrenia and chromosomal fragile sites.
[electronic resource]
by
Garofalo, G
Ragusa, R M
Barletta, C
Spina, E
Producer:
19920826
In:
The American journal of psychiatry
vol. 149
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484.
Direct intrachromosomal duplication of 16q and heritable fragile site fra (10) (q25) in the same patient.
[electronic resource]
by
Romain, D R
Frazer, A G
Columbano-Green, L M
Parfitt, R G
Smythe, R H
Chapman, C J
Producer:
19850103
In:
American journal of medical genetics
vol. 19
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485.
[Chromosome instability syndromes].
[electronic resource]
by
Germain, D
Bernheim, A
Producer:
19830311
In:
Pathologie-biologie
vol. 30
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486.
A new family with fra(10)(q25): spontaneous expression and 100% expression with 100 microM BrdU.
[electronic resource]
by
Gollin, S M
Bock, H G
Caskey, C T
Ledbetter, D H
Producer:
19850924
In:
American journal of medical genetics
vol. 21
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487.
Haemopoietic stem/progenitor cell transplant in Fanconi anaemia using HLA-matched sibling umbilical cord blood cells.
[electronic resource]
by
Kohli-Kumar, M
Shahidi, N T
Broxmeyer, H E
Masterson, M
Delaat, C
Sambrano, J
Morris, C
Auerbach, A D
Harris, R E
Producer:
19940215
In:
British journal of haematology
vol. 85
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488.
Stability and haplotype analysis of the FRAXE region.
[electronic resource]
by
Murray, A
Ennis, S
Youings, S A
Sharrock, A J
Lewis, C
Pound, M C
Macpherson, J N
Dennis, N R
Morton, N E
Jacobs, P A
Producer:
20001207
In:
European journal of human genetics : EJHG
vol. 8
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489.
Different mechanisms in the tumorigenesis of proximal and distal colon cancers.
[electronic resource]
by
Lindblom, A
Producer:
20010215
In:
Current opinion in oncology
vol. 13
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490.
Detection of a novel chromosomal translocation and chromosomal instability in women with recurrent abortions.
[electronic resource]
by
Alkhalaf, Moussa
Producer:
20071218
In:
The Journal of reproductive medicine
vol. 52
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491.
Three infants having null acute lymphoblastic leukemia with chromosome rearrangements at 11q23: no involvement of a heritable fragile site in this band.
[electronic resource]
by
van den Berghe, J A
Malcolm, S
Katz, F E
Gibbons, B
Czepulkowski, B
Chessells, J M
Producer:
19890823
In:
Cytogenetics and cell genetics
vol. 50
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492.
Fragile site expression in families with von Hippel-Lindau disease.
[electronic resource]
by
Jordan, D K
Divelbiss, J E
Waziri, M H
Burns, T L
Patil, S R
Producer:
19890905
In:
Cancer genetics and cytogenetics
vol. 39
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493.
Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients.
[electronic resource]
by
Jaspers, N G
Gatti, R A
Baan, C
Linssen, P C
Bootsma, D
Producer:
19890711
In:
Cytogenetics and cell genetics
vol. 49
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494.
[Refractory anemia with excess of blasts in transformation with heritable fragile site: a case report].
[electronic resource]
by
Nagashima, M
Suzuki, J
Aoyama, A
Tsuji, M
Bessho, M
Saito, M
Hirashima, K
Minamihisamatsu, M
Producer:
19880804
In:
[Rinsho ketsueki] The Japanese journal of clinical hematology
vol. 29
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495.
Paternal non-disjunction in a 46,XY/47,XXY individual with a fragile 17p12 in the mother.
[electronic resource]
by
Tommerup, N
Tønnesen, T
Gustavson, K H
Producer:
19861118
In:
Clinical genetics
vol. 30
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496.
Expression of folate-sensitive fragile sites in lymphocyte chromosomes.
[electronic resource]
by
Fuster, C
Miró, R
Templado, C
Barrios, L
Egozcue, J
Producer:
19890407
In:
Human genetics
vol. 81
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497.
Detection of the fragile X chromosome and other fragile sites.
[electronic resource]
by
Hecht, F
Sutherland, G R
Producer:
19850110
In:
Clinical genetics
vol. 26
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498.
Fra(10)(q25): the BrdU effect is substitution-dependent.
[electronic resource]
by
Gollin, S M
Holmquist, G P
Ledbetter, D H
Producer:
19850325
In:
American journal of human genetics
vol. 37
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499.
Co-cultivation studies in the expression of fragile (X) (q27) in lymphocytes.
[electronic resource]
by
Webb, T P
Producer:
19850925
In:
Clinical genetics
vol. 27
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500.
Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28.
[electronic resource]
by
Ritchie, R J
Chakrabarti, L
Knight, S J
Harding, R M
Davies, K E
Producer:
19980202
In:
American journal of medical genetics
vol. 73
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