Pages that link to "Q55670526"
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The following pages link to Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy (Q55670526):
Displaying 50 items.
- myotonic dystrophy (Q1860507) (← links)
- Psychostimulants for hypersomnia (excessive daytime sleepiness) in myotonic dystrophy (Q24245250) (← links)
- Isolation of the human genomic brain-2/N-Oct 3 gene (POUF3) and assignment to chromosome 6q16 (Q24317240) (← links)
- Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophy (Q24328773) (← links)
- Muscle channelopathies and critical points in functional and genetic studies (Q24532297) (← links)
- Comparative genomics and molecular dynamics of DNA repeats in eukaryotes (Q24650948) (← links)
- Altered phosphorylation and intracellular distribution of a (CUG)n triplet repeat RNA-binding protein in patients with myotonic dystrophy and in myotonin protein kinase knockout mice (Q24654728) (← links)
- The heart and cardiac pacing in Steinert disease (Q26825549) (← links)
- Molecular genetics and genetic testing in myotonic dystrophy type 1. (Q27691417) (← links)
- Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease (Q28208062) (← links)
- Gastric emptying in myotonic dystrophy (Q28218740) (← links)
- CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1 (Q28235526) (← links)
- Alternative splicing of myomesin 1 gene is aberrantly regulated in myotonic dystrophy type 1 (Q28244232) (← links)
- Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p (Q28250966) (← links)
- Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) (Q28250990) (← links)
- Chromosomal distribution of 320 genes from a brain cDNA library (Q28264122) (← links)
- Calcium-activated potassium channels (Q28278153) (← links)
- Biological Efficacy and Toxicity of Diamidines in Myotonic Dystrophy Type 1 Models. (Q30377390) (← links)
- Ultrasound-enhanced delivery of morpholino with Bubble liposomes ameliorates the myotonia of myotonic dystrophy model mice (Q30452003) (← links)
- Mouse homologues of human hereditary disease. (Q30495383) (← links)
- A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity (Q30495392) (← links)
- Immunolocalization of myotonic dystrophy protein kinase in corbular and junctional sarcoplasmic reticulum of human cardiac muscle (Q32062106) (← links)
- Relation of CTG expansion and clinical variables to electrocardiogram conduction abnormalities and sudden death in patients with myotonic dystrophy (Q33150808) (← links)
- Accurate characterization of the tyrosine hydroxylase forensic allele 9.3 through development of electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (Q33178471) (← links)
- Usefulness of clinical and electrocardiographic data for predicting adverse cardiac events in patients with myotonic dystrophy (Q33408844) (← links)
- Genetic anticipation and musculoskeletal disease (Q33566842) (← links)
- Targeting toxic RNAs that cause myotonic dystrophy type 1 (DM1) with a bisamidinium inhibitor (Q33588831) (← links)
- Instability versus predictability: the molecular diagnosis of myotonic dystrophy (Q33594617) (← links)
- Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations (Q33594622) (← links)
- Minimal expression of myotonic dystrophy: a clinical and molecular analysis (Q33594628) (← links)
- The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy (Q33594634) (← links)
- Presymptomatic diagnosis of myotonic dystrophy (Q33594647) (← links)
- Expansion of the myotonic dystrophy gene in Italian and Spanish patients. (Q33594657) (← links)
- A study of DNA methylation in myotonic dystrophy (Q33595060) (← links)
- A specific mutation for Huntington's disease (Q33596040) (← links)
- Dynamic mutations on the move (Q33596046) (← links)
- Gametic but not somatic instability of CAG repeat length in Huntington's disease. (Q33596051) (← links)
- Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range (Q33596071) (← links)
- The natural history of congenital myotonic dystrophy: mortality and long term clinical aspects (Q33623147) (← links)
- French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion (Q33672778) (← links)
- Intelligence quotient profile in myotonic dystrophy, intergenerational deficit, and correlation with CTG amplification (Q33673856) (← links)
- A case of paternally inherited congenital myotonic dystrophy (Q33674182) (← links)
- Anticipation resulting in elimination of the myotonic dystrophy gene: a follow up study of one extended family (Q33674709) (← links)
- Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 Brazilian families. (Q33675462) (← links)
- Contribution of molecular analyses to the estimation of the risk of congenital myotonic dystrophy. (Q33675728) (← links)
- Ascertainment of myotonic dystrophy through cataract by selective screening (Q33677080) (← links)
- Homozygous myotonic dystrophy: clinical and molecular studies of three unrelated cases (Q33677815) (← links)
- Segregation distortion of the CTG repeats at the myotonic dystrophy (DM) locus: new data from Brazilian DM families (Q33679504) (← links)
- Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats (Q33680162) (← links)
- Knowledge, views, and experience of 25 women with myotonic dystrophy (Q33681703) (← links)