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Results of search for 'su:"Chromosome Fragility"', page 31 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
601.
Abnormal FHIT transcripts in human breast carcinomas: a clinicopathological and epidemiological analysis of 61 Japanese cases.
[electronic resource]
by
Hayashi, S
Tanimoto, K
Hajiro-Nakanishi, K
Tsuchiya, E
Kurosumi, M
Higashi, Y
Imai, K
Suga, K
Nakachi, K
Producer:
19970610
In:
Cancer research
vol. 57
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602.
Genetic predisposition to retinoblastoma (Rb).
[electronic resource]
by
Zheng, Y
Tang, D
Peng, H
Producer:
19940601
In:
Yan ke xue bao = Eye science
vol. 9
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603.
B-cell lymphoma following polycythemia vera: evidence for the involvement of two different clones.
[electronic resource]
by
Schlaifer, D
Dastugue, N
Brousset, P
Delsol, G
Muller, C
Rigal-Huguet, F
Attal, M
Laurent, G
Pris, J
Producer:
19940610
In:
Leukemia
vol. 8
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604.
[A cytogenic study on colorectal carcinoma].
[electronic resource]
by
Wang, B
Yin, P
Kong, L
Producer:
19990325
In:
Zhonghua bing li xue za zhi = Chinese journal of pathology
vol. 26
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605.
Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome.
[electronic resource]
by
Silahtaroglu, A
Hol, F A
Jensen, P K
Erdel, M
Duba, H C
Geurds, M P
Knoers, N V
Mariman, E C
Tümer, Z
Utermann, G
Wirth, J
Bugge, M
Tommerup, N
Producer:
19990513
In:
European journal of human genetics : EJHG
vol. 7
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606.
Understanding replication fork progression, stability, and chromosome fragility by exploiting the Suppressor of Underreplication protein.
[electronic resource]
by
Nordman, Jared T
Orr-Weaver, Terry L
Producer:
20160119
In:
BioEssays : news and reviews in molecular, cellular and developmental biology
vol. 37
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607.
Identification of a break-prone structure in the 9q1 heterochromatic region.
[electronic resource]
by
Mamuris, Z
Aurias, A
Dutrillaux, B
Producer:
19910402
In:
Human genetics
vol. 86
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608.
The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X.
[electronic resource]
by
Sutherland, G R
Baker, E
Producer:
19900516
In:
Clinical genetics
vol. 37
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609.
Common fragile sites in couples with recurrent spontaneous abortions.
[electronic resource]
by
Schlegelberger, B
Gripp, K
Grote, W
Producer:
19890519
In:
American journal of medical genetics
vol. 32
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610.
Cancer in relatives of leukemic patients with chromosomal rearrangements at rare (heritable) fragile-site locations in their malignant cells.
[electronic resource]
by
Mules, E H
Testa, J R
Thomas, G H
Abbey, H
Cohen, B H
Producer:
19890628
In:
American journal of human genetics
vol. 44
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611.
Interstitial deletion of chromosome 3p: report of a patient and delineation of a proximal 3p deletion syndrome.
[electronic resource]
by
Neri, G
Reynolds, J F
Westphal, J
Hinz, J
Daniel, A
Producer:
19841212
In:
American journal of medical genetics
vol. 19
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612.
Recombination of DXS548 (RS46) with the FRAXA locus.
[electronic resource]
by
Dreesen, J C
Smits, A P
van Oost, B A
Producer:
19941116
In:
American journal of medical genetics
vol. 51
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613.
Brachydactyly and fragile site at 16q22: a chance association.
[electronic resource]
by
Rivera, H
Producer:
19980710
In:
Genetic counseling (Geneva, Switzerland)
vol. 9
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614.
Apolipoprotein B genetic variability in Brazilian Indians.
[electronic resource]
by
Kaufman, L
Vargas, A F
Coimbra Júnior, C E
Santos, R V
Salzano, F M
Hutz, M H
Producer:
19990305
In:
Human biology
vol. 71
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615.
Genome-wide screen identifies pathways that govern GAA/TTC repeat fragility and expansions in dividing and nondividing yeast cells.
[electronic resource]
by
Zhang, Yu
Shishkin, Alexander A
Nishida, Yuri
Marcinkowski-Desmond, Dana
Saini, Natalie
Volkov, Kirill V
Mirkin, Sergei M
Lobachev, Kirill S
Producer:
20130403
In:
Molecular cell
vol. 48
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616.
Limited size of the fragile X site shown by fluorescence in situ hybridization.
[electronic resource]
by
Verkerk, A J
Eussen, B H
Van Hemel, J O
Oostra, B A
Producer:
19920716
In:
American journal of medical genetics
vol. 43
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617.
Clonal duplication of the Y chromosome and fra(X)(q28) in a case of epidermoid carcinoma of the esophagus.
[electronic resource]
by
Casalone, R
Minelli, E
Portensoso, P
Giudici, A
Producer:
19900503
In:
Cancer genetics and cytogenetics
vol. 45
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618.
The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation.
[electronic resource]
by
Proops, R
Webb, T
Producer:
19820412
In:
Journal of medical genetics
vol. 18
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619.
[Genetic aspects of autosomal fragile sites. Apropos of 40 Cases].
[electronic resource]
by
Guichaoua, M
Matteï, M G
Matteï, J F
Giraud, F
Producer:
19830311
In:
Journal de genetique humaine
vol. 30
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620.
Centromere spreading in a case of megaloblastic anemia "cured" under TC 199 culture conditions.
[electronic resource]
by
Bamezai, R
Shiraishi, Y
Taguchi, H
Producer:
19860313
In:
Cancer genetics and cytogenetics
vol. 20
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