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Results of search for 'su:"Chromosome Fragility"', page 37 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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721.
[Fragile X syndrome].
[electronic resource]
by
Yamagata, T
Producer:
19980709
In:
Ryoikibetsu shokogun shirizu
no. 18 Pt 1
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722.
Fragile site and interstitial telomere repeat sequences at the fusion point of a de novo (Y;13) translocation.
[electronic resource]
by
Boutouil, M
Fetni, R
Qu, J
Dallaire, L
Richer, C L
Lemieux, N
Producer:
19960912
In:
Human genetics
vol. 98
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723.
Detection of fragile sites induced by pyrimethamine.
[electronic resource]
by
Egeli, U
Tunca, B
Producer:
19970924
In:
Teratogenesis, carcinogenesis, and mutagenesis
vol. 17
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724.
Genetic alterations in cancer as a result of breakage at fragile sites.
[electronic resource]
by
Popescu, Nicholas C
Producer:
20030530
In:
Cancer letters
vol. 192
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725.
Differential expression of FRA16B in peripheral lymphocytes and bone marrow cells.
[electronic resource]
by
Zollino, M
Genuardi, M
Neri, G
Producer:
19901114
In:
Cancer genetics and cytogenetics
vol. 49
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726.
Distribution of autosomal fragile sites in specimens cultured for prenatal fragile X diagnosis.
[electronic resource]
by
Krawczun, M S
Jenkins, E C
Duncan, C J
Stark-Houck, S L
Kunaporn, S
Schwatz-Richstein, C
Gu, H
Brown, W T
Producer:
19910521
In:
American journal of medical genetics
vol. 38
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727.
Fragile sites and spontaneous abortions.
[electronic resource]
by
Toncheva, D
Producer:
19920421
In:
Genetic counseling (Geneva, Switzerland)
vol. 2
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728.
Fragile sites and X-linked retardation.
[electronic resource]
by
Hecht, F
Hecht, B K
Glover, T W
Producer:
19820322
In:
Hospital practice (Office ed.)
vol. 16
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729.
Is Rett syndrome a chromosome breakage syndrome?
[electronic resource]
by
Telvi, L
Leboyer, M
Chiron, C
Feingold, J
Ponsot, G
Producer:
19941116
In:
American journal of medical genetics
vol. 51
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730.
Benign chronic neutropenia with abnormalities involving 16q22, affecting mother and daughter.
[electronic resource]
by
Glasser, Lewis
Meloni-Ehrig, Aurelia
Joseph, Plakyil
Mendiola, Jennifer
Producer:
20060522
In:
American journal of hematology
vol. 81
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731.
Chromatin changes in the development and pathology of the Fragile X-associated disorders and Friedreich ataxia.
[electronic resource]
by
Kumari, Daman
Lokanga, Rachel
Yudkin, Dmitry
Zhao, Xiao-Nan
Usdin, Karen
Producer:
20130402
In:
Biochimica et biophysica acta
vol. 1819
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732.
[Philadelphia chromosome-positive adult acute lymphocytic leukemia].
[electronic resource]
by
Morioka, M
Okabe, M
Producer:
19910812
In:
[Rinsho ketsueki] The Japanese journal of clinical hematology
vol. 32
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733.
A population cytogenetic study of a common fragile site, fra(3)(p14), in a healthy population.
[electronic resource]
by
Murata, M
Otsuka, M
Hayakawa, Y
Takahashi, E
Tsuji, H
Hori, T
Producer:
19910703
In:
Jinrui idengaku zasshi. The Japanese journal of human genetics
vol. 35
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734.
Fragile (X) expression induced by FUdR is transient and inversely related to levels of thymidylate synthase activity.
[electronic resource]
by
Cantú, E S
Nussbaum, R L
Airhart, S D
Ledbetter, D H
Producer:
19851031
In:
American journal of human genetics
vol. 37
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735.
Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3.
[electronic resource]
by
Patterson, M
Bell, M
Schwartz, C
Davies, K
Producer:
19881108
In:
American journal of medical genetics
vol. 30
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736.
Chromosome breaks and fragile sites in leukemic bone marrow cells.
[electronic resource]
by
Przylepa, K A
Wenger, S L
Producer:
19880803
In:
Cancer genetics and cytogenetics
vol. 33
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737.
Regional localization for HLA by recombination with a fragile site at 6p23.
[electronic resource]
by
Mulley, J C
Hay, J
Sheffield, L J
Sutherland, G R
Producer:
19840107
In:
American journal of human genetics
vol. 35
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738.
Chromosome fragility in patients with sporadic unilateral retinoblastoma.
[electronic resource]
by
de Nuñez, M
Penchaszadeh, V B
Pimentel, E
Producer:
19840321
In:
Cancer genetics and cytogenetics
vol. 11
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739.
A deleted chromosome no. 13 in human retinoblastoma cells: relevance to tumorigenesis.
[electronic resource]
by
Balaban-Malenbaum, G
Gilbert, F
Nichols, W W
Hill, R
Shields, J
Meadows, A T
Producer:
19811215
In:
Cancer genetics and cytogenetics
vol. 3
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740.
Heritable fragile sites on human chromosomes. XII. Population cytogenetics.
[electronic resource]
by
Sutherland, G R
Producer:
19860108
In:
Annals of human genetics
vol. 49
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