id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_gdtdtq7ggre7jcsxoru73qy7gi	N T Potter	Meiotic instability associated with the CAGR1 trinucleotide repeat at 13q13	1997.0	3	.pdf	application/pdf	2065	384	69	CAGR1 is a recently characterised polymorphic trinucleotide repeat localised to 13qI3, which has been suggested as a possible candidate gene for neurological disorders that manifest genetic anticipation. CAGR1 repeat number of 50 was identified (normal range 9-29). CAG alleles and meiotic instability of Keywords: CAGRI; trinucleotide repeat; meiotic instability screening a human retinal cDNA library, identified a highly polymorphic CAG repeat (called brain (cerebellum), and their subsequent identification of a single allele with 46 repeats in a candidate gene for molecularly uncharacterised inherited neurodegenerative, neuropsychiatric, or neurodevelopmental disorders. inheritance ofCAGR1 repeats in the normal range through 14 meioses in t 928 chromosomes were studied for the determination of CAGRI repeat number. of CAG repeat lengths in the normal range (fig Meiotic instability associated with the CAGRI trinucleotide repeat at 13q13 CAG repeats in schizophrenia and bipolar disorder. Novel triplet repeat containing genes in human brain: location and analysis of a highly polymorphic (CAG)n trinucleotide repeat.	./cache/work_gdtdtq7ggre7jcsxoru73qy7gi.pdf	./txt/work_gdtdtq7ggre7jcsxoru73qy7gi.txt