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Results of search for 'su:"Chromosome Fragility"', page 41 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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801.
A high resolution deletion map of human chromosome Xp22.
[electronic resource]
by
Schaefer, L
Ferrero, G B
Grillo, A
Bassi, M T
Roth, E J
Wapenaar, M C
van Ommen, G J
Mohandas, T K
Rocchi, M
Zoghbi, H Y
Ballabio, A
Producer:
19930924
In:
Nature genetics
vol. 4
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802.
The morbid cutaneous anatomy of the human genome.
[electronic resource]
by
Epstein, E H
Producer:
19931214
In:
Archives of dermatology
vol. 129
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803.
Human chromosome fragility.
[electronic resource]
by
Lukusa, T
Fryns, J P
Producer:
20080619
In:
Biochimica et biophysica acta
vol. 1779
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804.
Cutis verticis gyrata and chromosomal fragile sites.
[electronic resource]
by
Musumeci, S A
Ferri, R
Viglianesi, M
Elia, M
Ragusa, R M
Bergonzi, P
Producer:
19910521
In:
American journal of medical genetics
vol. 38
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805.
Common fragile sites and human cancer. A study on lymphocytes from neuroblastoma patients.
[electronic resource]
by
Vernole, P
Tedeschi, B
Caporossi, D
Nicoletti, B
Producer:
19890202
In:
Cancer genetics and cytogenetics
vol. 36
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806.
Spontaneous expression of fra(10)(q25) in bone marrow from a patient with agranulocytosis.
[electronic resource]
by
Haney, S M
Butler, F O
Heerema, N A
Producer:
19890406
In:
American journal of medical genetics
vol. 31
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807.
Fragile sites are unrelated to reciprocal translocation breakpoints.
[electronic resource]
by
Davis, J R
Hagaman, R M
Producer:
19870828
In:
Clinical genetics
vol. 31
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808.
The fragile X syndromes.
[electronic resource]
by
Nelson, D L
Producer:
19950831
In:
Seminars in cell biology
vol. 6
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809.
Spontaneous expression of the chromosome fragile site fra(10)(q25).
[electronic resource]
by
Taylor, A M
Bundey, S
Producer:
19830324
In:
American journal of human genetics
vol. 35
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810.
Interstitial telomere DNA sequences are not detectable at breaking sites of classical heritable fragile sites.
[electronic resource]
by
Petit, P
Producer:
19970325
In:
Human genetics
vol. 99
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811.
Chromosome imbalance at the 3p14 region in human breast tumours: high frequency in patients with inherited predisposition due to BRCA2.
[electronic resource]
by
Bergthorsson, J T
Johannsdottir, J
Jonasdottir, A
Eiriksdottir, G
Egilsson, V
Ingvarsson, S
Barkardottir, R B
Arason, A
Producer:
19980618
In:
European journal of cancer (Oxford, England : 1990)
vol. 34
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812.
Chromosome fragile sites in mentally retarded males: increased incidence with seizures and diphenylhydantoin therapy.
[electronic resource]
by
Hodges, K B
Larson, R S
Butler, M G
Producer:
19981207
In:
Annals of clinical and laboratory science
vol. 28
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813.
Transfected c-Ha-ras oncogene enhances karyotypic instability and integrates predominantly in aberrant chromosomes.
[electronic resource]
by
de Vries, J E
Kornips, F H
Marx, P
Bosman, F T
Geraedts, J P
ten Kate, J
Producer:
19930706
In:
Cancer genetics and cytogenetics
vol. 67
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814.
X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers.
[electronic resource]
by
Nielsen, K B
Tommerup, N
Poulsen, H
Mikkelsen, M
Producer:
20000606
In:
Human genetics
vol. 59
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815.
Molecular biology: DNA fragility put into context.
[electronic resource]
by
Huebner, Kay
Producer:
20110222
In:
Nature
vol. 470
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816.
Expression of fra(10)(q25) in peripheral blood and bone marrow in familial neutropenia.
[electronic resource]
by
Holmes, J A
Thompson, P W
Producer:
19880616
In:
Journal of medical genetics
vol. 25
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817.
Heritable fragile sites and cancer: fra(16)(q22) in lymphocytes of an acute nonlymphocytic leukemia patient with inv(16)(p13q22).
[electronic resource]
by
Murata, M
Takahashi, E
Ishihara, T
Minamihisamatsu, M
Takagi, T
Kaneko, Y
Hori, T
Producer:
19870318
In:
Cancer genetics and cytogenetics
vol. 25
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818.
The effect of methionine and 5-azacytidine on fragile X expression.
[electronic resource]
by
Abruzzo, M A
Mayer, M
Jacobs, P A
Producer:
19850325
In:
American journal of human genetics
vol. 37
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819.
A cytogenetic survey of a mentally retarded school-age population with special reference to fragile sites.
[electronic resource]
by
Webb, T P
Thake, A I
Bundey, S E
Todd, J
Producer:
19870714
In:
Journal of mental deficiency research
vol. 31 ( Pt 1)
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820.
Cytogenetic t(11;17)(q13;q21) in a pediatric ependymoma. Is 11q13 a recurring breakpoint in ependymomas?
[electronic resource]
by
Sainati, L
Montaldi, A
Putti, M C
Giangaspero, F
Rigobello, L
Stella, M
Zanesco, L
Basso, G
Producer:
19920612
In:
Cancer genetics and cytogenetics
vol. 59
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