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	61.	Refinement of the spinal muscular atrophy locus by genetic and physical mapping. [electronic resource] by Wang, C H Kleyn, P W Vitale, E Ross, B M Lien, L Xu, J Carter, T A Brzustowicz, L M Obici, S Selig, S Producer: 19950213 In: American journal of human genetics vol. 56 Availability: No items available. Save to lists Add to cart (remove)
	62.	Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy. [electronic resource] by Wang, C H Xu, J Carter, T A Ross, B M Dominski, M K Bellcross, C A Penchaszadeh, G K Munsat, T L Gilliam, T C Producer: 19970113 In: Human molecular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	Construction of a yeast artificial chromosome contig spanning the spinal muscular atrophy disease gene region. [electronic resource] by Kleyn, P W Wang, C H Lien, L L Vitale, E Pan, J Ross, B M Grunn, A Palmer, D A Warburton, D Brzustowicz, L M Producer: 19930830 In: Proceedings of the National Academy of Sciences of the United States of America vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Brain glyceraldehyde-3-phosphate dehydrogenase activity in human trinucleotide repeat disorders. [electronic resource] by Kish, S J Lopes-Cendes, I Guttman, M Furukawa, Y Pandolfo, M Rouleau, G A Ross, B M Nance, M Schut, L Ang, L DiStefano, L Producer: 19981125 In: Archives of neurology vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	The human nucleus accumbens is highly susceptible to G protein down-regulation by methamphetamine and heroin. [electronic resource] by McLeman, E R Warsh, J J Ang, L Li, P P Kalasinsky, K S Ross, B M Tong, J Schmunk, G Adams, V Kish, S J Producer: 20000525 In: Journal of neurochemistry vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3. [electronic resource] by Banerjee, P Lewis, C A Kleyn, P W Shugart, Y Y Ross, B M Penchaszadeh, G K Ott, J Jacobson, S G Gilliam, T C Knowles, J A Producer: 19980608 In: Genomics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	67.	Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease. [electronic resource] by Clark, L N Ross, B M Wang, Y Mejia-Santana, H Harris, J Louis, E D Cote, L J Andrews, H Fahn, S Waters, C Ford, B Frucht, S Ottman, R Marder, K Producer: 20071015 In: Neurology vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa. [electronic resource] by Banerjee, P Kleyn, P W Knowles, J A Lewis, C A Ross, B M Parano, E Kovats, S G Lee, J J Penchaszadeh, G K Ott, J Jacobson, S G Gilliam, T C Producer: 19980224 In: Nature genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions. [electronic resource] by Carter, T A Bönnemann, C G Wang, C H Obici, S Parano, E De Fatima Bonaldo, M Ross, B M Penchaszadeh, G K Mackenzie, A Soares, M B Kunkel, L M Gilliam, T C Producer: 19970827 In: Human molecular genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	70.	Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses. [electronic resource] by Shah, A B Chernov, I Zhang, H T Ross, B M Das, K Lutsenko, S Parano, E Pavone, L Evgrafov, O Ivanova-Smolenskaya, I A Annerén, G Westermark, K Urrutia, F H Penchaszadeh, G K Sternlieb, I Scheinberg, I H Gilliam, T C Petrukhin, K Producer: 19971015 In: American journal of human genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)