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Results of search for 'su:"Chromosome Fragility"', page 30 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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581.
Fragility of the centromeric region of chromosome 1 associated with combined immunodeficiency in siblings. A recessively inherited entity?
[electronic resource]
by
Fasth, A
Forestier, E
Holmberg, E
Holmgren, G
Nordenson, I
Söderström, T
Wahlström, J
Producer:
19900918
In:
Acta paediatrica Scandinavica
vol. 79
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582.
Different inducibility and possible significance of several concomitant "fragile sites" in two brothers.
[electronic resource]
by
Shabtai, F
Orlin, J
Hart, J
Halbrecht, I
Klar, D
Friedman, J
Producer:
19861030
In:
Human genetics
vol. 74
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583.
FRA2B is distinct from inverted telomere repeat arrays at 2q13.
[electronic resource]
by
IJdo, J W
Baldini, A
Wells, R A
Ward, D C
Reeders, S T
Producer:
19920529
In:
Genomics
vol. 12
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584.
Spontaneous and induced chromosome aberrations in Balkan endemic nephropathy.
[electronic resource]
by
Toncheva, D I
Gergov, T D
Tzoneva, M T
Bouchakliev, Z P
Producer:
19920213
In:
Kidney international. Supplement
vol. 34
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585.
Chromosome fragility in the Lennox-Gastaut epilepsy syndrome.
[electronic resource]
by
Smith, A
Beran, R G
Producer:
19930108
In:
Journal of intellectual disability research : JIDR
vol. 36 ( Pt 5)
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586.
Retinoblastoma: clinical observations and histopathological study.
[electronic resource]
by
Sang, D N
Albert, D M
Kuo, P K
Producer:
19821021
In:
International ophthalmology clinics
vol. 22
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587.
Unusual behaviour of a human autosome having two rare folate sensitive fragile sites.
[electronic resource]
by
Sutherland, G R
Baker, E
Producer:
19940328
In:
Annales de genetique
vol. 36
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588.
Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypes.
[electronic resource]
by
Estop, A M
Bansal, V
Lin, A
Levinson, F
Karlin, S M
Surti, U
Wenger, S L
Steele, M W
Producer:
19940517
In:
American journal of medical genetics
vol. 49
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589.
Sequence of the FRA3B common fragile region: implications for the mechanism of FHIT deletion.
[electronic resource]
by
Inoue, H
Ishii, H
Alder, H
Snyder, E
Druck, T
Huebner, K
Croce, C M
Producer:
19980202
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 94
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590.
DNA repeat expansions and human disease.
[electronic resource]
by
Usdin, K
Grabczyk, E
Producer:
20000831
In:
Cellular and molecular life sciences : CMLS
vol. 57
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591.
Oncogenes create a unique landscape of fragile sites.
[electronic resource]
by
Miron, Karin
Golan-Lev, Tamar
Dvir, Raz
Ben-David, Eyal
Kerem, Batsheva
Producer:
20160506
In:
Nature communications
vol. 6
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592.
New common fragile sites.
[electronic resource]
by
Hecht, F
Tajara, E H
Lockwood, D
Sandberg, A A
Hecht, B K
Producer:
19880803
In:
Cancer genetics and cytogenetics
vol. 33
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593.
[Genetic and cytogenetic characteristics of human neuroblastoma].
[electronic resource]
by
Vernole, P
Melino, G
Producer:
19890203
In:
La Clinica terapeutica
vol. 124
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594.
High-resolution chromosome banding and fragile site studies in von Hippel-Lindau syndrome.
[electronic resource]
by
Neumann, H P
Schempp, W
Wienker, T F
Producer:
19880408
In:
Cancer genetics and cytogenetics
vol. 31
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595.
Feasibility of fragile X chromosome prenatal diagnosis demonstrated.
[electronic resource]
by
Jenkins, E C
Brown, W T
Duncan, C J
Brooks, J
Ben-Yishay, M
Giordano, F M
Nitowsky, H M
Producer:
19820222
In:
Lancet (London, England)
vol. 2
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596.
[Unstable DNA sequence and methylation in fragile X syndrome].
[electronic resource]
by
Fu, S D
Shen, Y
Fan, Y
Producer:
19950309
In:
Zhonghua yi xue za zhi
vol. 74
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597.
[A common link in the mechanism of the self-maintenance of malignant growth: the syndrome of the nonhealing wound].
[electronic resource]
by
Luchnik, A N
Producer:
20000914
In:
Ontogenez
vol. 31
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598.
Distribution of intrachromosomal telomeric sequences (ITS) on Macaca fascicularis (Primates) chromosomes and their implication for chromosome evolution.
[electronic resource]
by
Ruiz-Herrera, A
García, F
Azzalin, C
Giulotto, E
Egozcue, J
Ponsà, M
Garcia, M
Producer:
20020813
In:
Human genetics
vol. 110
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599.
Autosomal folate sensitive fragile sites in an autistic Basque sample.
[electronic resource]
by
Arrieta, I
Nuñez, T
Gil, A
Flores, P
Usobiaga, E
Martinez, B
Producer:
19961107
In:
Annales de genetique
vol. 39
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600.
Analysis of triplet repeats of the FRAXA locus using a novel sequencing procedure.
[electronic resource]
by
Barlati, S
Belletti, L
Gardella, R
Ferraboli, S
Producer:
19970113
In:
Acta geneticae medicae et gemellologiae
vol. 45
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