id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_peoi6idm4bd3nc7qwgzelsautu	Kym M. Boycott	Evidence for Genetic Heterogeneity in X-Linked Congenital Stationary Night Blindness	1998	11	.pdf	application/pdf	7714	639	65	Mb. Genetic and clinical analyses of this set of 32 families with X-linked CSNB, together with the family studies reported in the literature, strongly suggest that two that a minimum of two loci for X-linked CSNB are possible: one proximal to DXS426 (Bech-Hansen et al. Figure 1 Fifteen recombination events in X chromosomes from nine families that segregate the complete form of X-linked CSNB. Figure 2 Eleven recombination events in X chromosomes from seven families that segregate the incomplete form of X-linked CSNB. carried a recombinant chromosome that successively positioned the CSNB2 gene proximal to TIMP1 (BechHansen and Pearce 1993), DXS426 (Bech-Hansen et al. individual from family 70 was reported to carry a recombinant chromosome that placed the CSNB2 gene Haplotype Analysis of 17 Families with Incomplete X-Linked CSNB refine the map position of CSNB2, we continued to investigate the recombinant chromosomes in these families, using new microsatellite markers, and we identified	./cache/work_peoi6idm4bd3nc7qwgzelsautu.pdf	./txt/work_peoi6idm4bd3nc7qwgzelsautu.txt