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Journal Name Change
Vol. 1-11 (1962-1972) were published under the journal's former title Cytogenetics and Vol. 12-95 (1973-2001) under Cytogenetics and Cell Genetics.
Cytogenetic and Genome Research 2003, Vol. 100, No. 1-4
Why is SCA12 different from other SCAs?
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 189–197.
https://doi.org/10.1159/000072854
Understanding fragile X syndrome: insights from animal models
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 111–123.
https://doi.org/10.1159/000072845
Preface
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 5–6.
https://doi.org/10.1159/000072835
Forgotten fragile sites and related phenomena
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 89–91.
https://doi.org/10.1159/000072842
Subject Index Vol. 100, 2003
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 297–298.
https://doi.org/10.1159/000073834
Author Index Vol. 100, 2003
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 296.
https://doi.org/10.1159/000073833
The epilepsy, the protease inhibitor and the dodecamer: progressive myoclonus epilepsy, cystatin b and a 12-mer repeat expansion
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 213–223.
https://doi.org/10.1159/000072857
FMR2 function: insight from a mouse knockout model
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 129–139.
https://doi.org/10.1159/000072847
The rare human fragile site 16B
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 85–88.
https://doi.org/10.1159/000072841
Title Page / Table of Contents
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 1–4.
https://doi.org/10.1159/000073832
Transgenic mouse models of spinal and bulbar muscular atrophy (SBMA)
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 243–251.
https://doi.org/10.1159/000072860
Instability of the fragile X syndrome repeat in mice: the effect of age, diet and mutations in genes that affect DNA replication, recombination and repair proficiency
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 140–146.
https://doi.org/10.1159/000072848
Transcription defects induced by repeat expansion: fragile X syndrome, FRAXE mental retardation, progressive myoclonus epilepsy type 1, and Friedreich ataxia
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 65–76.
https://doi.org/10.1159/000072839
Spontaneous chromosome loss and colcemid resistance in lymphocytes from patients with myotonic dystrophy type 1
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 224–229.
https://doi.org/10.1159/000072858
Spinocerebellar ataxia type 6 and episodic ataxia type 2: differences and similarities between two allelic disorders
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 147–153.
https://doi.org/10.1159/000072849
Common fragile sites
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 92–100.
https://doi.org/10.1159/000072843
Spinocerebellar ataxia 7 (SCA7)
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 154–163.
https://doi.org/10.1159/000072850
Trinucleotide repeat instability: a hairpin curve at the crossroads of replication, recombination, and repair
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 7–24.
https://doi.org/10.1159/000072836
Oculopharyngeal muscular dystrophy: a late-onset polyalanine disease
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 252–260.
https://doi.org/10.1159/000072861
Insights into the molecular basis of polyglutamine neurodegeneration from studies of a spinocerebellar ataxia type 7 mouse model
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 164–174.
https://doi.org/10.1159/000072851
Rare fragile sites
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 77–84.
https://doi.org/10.1159/000072840
Molecular analyses of Machado-Joseph disease
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 261–275.
https://doi.org/10.1159/000072862
Reactivation of silenced genes and transcriptional therapy
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 56–64.
https://doi.org/10.1159/000072838
SCA10 and ATTCT repeat expansion: clinical features and molecular aspects
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 184–188.
https://doi.org/10.1159/000072853
WWOX, the common chromosomal fragile site, FRA16D, cancer gene
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 101–110.
https://doi.org/10.1159/000072844
Mechanisms of neuronal cell death in Huntington’s disease
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 287–295.
https://doi.org/10.1159/000072864
The hereditary spinocerebellar ataxias in Japan
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 198–205.
https://doi.org/10.1159/000072855
Expression of the FMR1 gene
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 124–128.
https://doi.org/10.1159/000072846
Contents Vol. 100, 2003
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 299.
https://doi.org/10.1159/000073835
A cerebellar tremor/ataxia syndrome among fragile X premutation carriers
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 206–212.
https://doi.org/10.1159/000072856
The contribution of cis-elements to disease-associated repeat instability: clinical and experimental evidence
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 25–55.
https://doi.org/10.1159/000072837
The use of transgenic and knock-in mice to study Huntington’s disease
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 276–286.
https://doi.org/10.1159/000072863
Molecular genetics of spinocerebellar ataxia type 8 (SCA8)
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 175–183.
https://doi.org/10.1159/000072852
Transgenic mouse models for myotonic dystrophy type 1 (DM1)
Subject Area:
Genetics
Cytogenet Genome Res (2003) 100 (1-4): 230–242.
https://doi.org/10.1159/000072859