Mutations: Unstable Repeat Expansions | Basicmedical Key
Absence of unidentified CAG repeat expansion in patients with Huntington's disease-like phenotype | Journal of Neurology, Neurosurgery & Psychiatry
Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease | Journal of Human Genetics
Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease | Journal of Human Genetics
Genetics of fetal anomalies (Chapter 1) - Fetal Medicine
The CAG repeat ranges and mean CAG numbers of the SBMA patients | Download Table
Genomic characteristics of CAG repeat diseases* | Download Table
Electropherogram results. A: Electropherogram of HD genotyping of... | Download Scientific Diagram
Translation of expanded CAG repeat mRNAs is regulated via the MID1... | Download Scientific Diagram
Trinucleotide repeat disorders: An interesting interface between psychiatry and medicine | BJPsych Advances | Cambridge Core
Huntington's disease (Chapter 6) - Neurogenetics
SciELO - Brasil - Huntington disease: DNA analysis in brazilian population Huntington disease: DNA analysis in brazilian population
Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease | Journal of Human Genetics
New NIST SRM Helps Improve Diagnosis of Huntington's Disease | NIST
Distribution of HTT CAG repeat sizes. The figure displays the frequency... | Download Scientific Diagram
a ) Genotypes (number of CAG repeats) and phenotypes: normal... | Download Scientific Diagram
PDF) Cag Repeat Expansion in Autosomal Dominant Pure Spastic Paraplegia Linked to Chromosome 2p21–p24
Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease | Journal of Human Genetics
Molecular Mechanisms Involved in the Pathogenesis of Huntington's Disease (Neurodegenerative Diseases-laboratory and Clinical Research): 9781617289712: Medicine & Health Science Books @ Amazon.com
Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat | Semantic Scholar
Microsatellite and trinucleotide repeat expansion diseases | HSTalks
a ) Genotypes (number of CAG repeats) and phenotypes: normal... | Download Scientific Diagram
Profiling of Short-Tandem-Repeat Disease Alleles in 12,632 Human Whole Genomes. - Abstract - Europe PMC
Profiling of Short-Tandem-Repeat Disease Alleles in 12,632 Human Whole Genomes. - Abstract - Europe PMC
