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	61.	Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophy. [electronic resource] by Yamaoka, L H Bartlett, R J Ross, D A Fey, G H Ledbetter, D H Bruns, G Pericak-Vance, M A Herbstreith, M H Roses, A D Producer: 19860131 In: Journal of neurogenetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	Prenatal diagnosis using deletion studies in Duchenne muscular dystrophy. [electronic resource] by Speer, M C Pericak-Vance, M A Yamaoka, L H Koh, J Hung, W Y Gaskell, P C Vance, J M Bartlett, R J Roses, A D Producer: 19890215 In: Prenatal diagnosis vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	Inherited deletion at Duchenne dystrophy locus in normal male. [electronic resource] by Bartlett, R J Walker, A P Laing, N G Koh, J Secore, S L Speer, M C Pericak-Vance, M Hung, W Y Yamaoka, L H Siddique, T Producer: 19890405 In: Lancet (London, England) vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Inherited deletion at Duchenne dystrophy locus in normal male. [electronic resource] by Koh, J Bartlett, R J Pericak-Vance, M A Speer, M C Yamaoka, L H Phillips, K Hung, W Y Ray, P N Worton, R G Gilbert, J R Producer: 19871216 In: Lancet (London, England) vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	A Bgl II polymorphism detected by LDR152 [D19S19]. [electronic resource] by Walker, A P Bartlett, R J Yamaoka, L H Secore, S L Lee, J E Gilbert, J Herbstreith, M Pericak-Vance, M A Hung, W Y Roses, A D Producer: 19881121 In: Nucleic acids research vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	A new tightly linked DNA probe for myotonic dystrophy. [electronic resource] by Roses, A D Pericak-Vance, M A Yamaoka, L H Herbstreith, M H Bartlett, R J Siddique, T Hung, W Y Ross, D A Mohandas, T K Bruns, G Producer: 19860917 In: Neurology vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	67.	Duchenne muscular dystrophy: high frequency of deletions. [electronic resource] by Bartlett, R J Pericak-Vance, M A Koh, J Yamaoka, L H Chen, J C Hung, W Y Speer, M C Wapenaar, M C Van Ommen, G J Bakker, E Producer: 19880216 In: Neurology vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphisms. [electronic resource] by Laing, N G Walker, A P Akkari, P A Chandler, D C Layton, M G Mears, M E Yamada, T Bartlett, R J Pericak-Vance, M A Hung, W Y Producer: 19910613 In: Prenatal diagnosis vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	Tight linkage of apolipoprotein C2 to myotonic dystrophy on chromosome 19. [electronic resource] by Pericak-Vance, M A Yamaoka, L H Assinder, R I Hung, W Y Bartlett, R J Stajich, J M Gaskell, P C Ross, D A Sherman, S Fey, G H Producer: 19861121 In: Neurology vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	70.	Prenatal detection of an inherited Duchenne muscular dystrophy deletion allele. [electronic resource] by Bartlett, R J Pericak-Vance, M A Lanman, J T Killam, A P Gilbert, J R Stajick, J M Chen, J C Siddique, T Kandt, R S Sirotkin-Roses, M Producer: 19870310 In: Neurology vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	Myotonic dystrophy: update on progress to define the gene. [electronic resource] by Roses, A D Pericak-Vance, M A Bartlett, R J Yamaoka, L H Lee, J E Koh, J Chen, J C Gilbert, J R Ross, D A Herbstreith, M H Producer: 19890126 In: Australian paediatric journal vol. 24 Suppl 1 Availability: No items available. Save to lists Add to cart (remove)
	72.	Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage. [electronic resource] by Pericak-Vance, M A Bebout, J L Gaskell, P C Yamaoka, L H Hung, W Y Alberts, M J Walker, A P Bartlett, R J Haynes, C A Welsh, K A Producer: 19910626 In: American journal of human genetics vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	73.	In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide. [electronic resource] by Bartlett, R J Stockinger, S Denis, M M Bartlett, W T Inverardi, L Le, T T thi Man, N Morris, G E Bogan, D J Metcalf-Bogan, J Kornegay, J N Producer: 20000925 In: Nature biotechnology vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	74.	Meeting of the Cell Transplantation Society in Miami. [electronic resource] by Partridge, T Beauchamp, J Morgan, J Tremblay, J P Huard, J Watt, D Wernig, A Irintchev, A Grounds, M Springer, M L Bartlett, R J Mendell, J Vilquin, J T Bower, J J Producer: 19970707 In: Cell transplantation vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	75.	Mutation segregation and rapid carrier detection of X-linked muscular dystrophy in dogs. [electronic resource] by Bartlett, R J Winand, N J Secore, S L Singer, J T Fletcher, S Wilton, S Bogan, D J Metcalf-Bogan, J R Bartlett, W T Howell, J M Cooper, B J Kornegay, J N Producer: 19961022 In: American journal of veterinary research vol. 57 Availability: No items available. Save to lists Add to cart (remove)