Your search returned 71 results.

Results
	41.	Studies on locus expansion, library representation, and chromosome walking using an efficient method to screen cosmid libraries. [electronic resource] by Bowden, D W Müller-Kahle, H Fulton, T R Gravius, T C Barker, D F Donis-Keller, H Producer: 19890404 In: Gene vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	Mutations in the codon for a conserved arginine-1563 in the COL4A5 collagen gene in Alport syndrome. [electronic resource] by Zhou, J Gregory, M C Hertz, J M Barker, D F Atkin, C Spencer, E S Tryggvason, K Producer: 19930422 In: Kidney international vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers. [electronic resource] by Dietz-Band, J N Turco, A E Willard, H F Vincent, A Skolnick, M H Barker, D F Producer: 19910213 In: Cytogenetics and cell genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3. [electronic resource] by Bennett, C L Yoshioka, R Kiyosawa, H Barker, D F Fain, P R Shigeoka, A O Chance, P F Producer: 20000330 In: American journal of human genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Multilocus mapping of the X-linked hypophosphatemic rickets gene. [electronic resource] by Econs, M J Barker, D F Speer, M C Pericak-Vance, M A Fain, P R Drezner, M K Producer: 19920731 In: The Journal of clinical endocrinology and metabolism vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Refined physical and genetic mapping of the NF1 region on chromosome 17. [electronic resource] by Fain, P R Goldgar, D E Wallace, M R Collins, F S Wright, E Nguyen, K Barker, D F Producer: 19891208 In: American journal of human genetics vol. 45 Availability: No items available. Save to lists Add to cart (remove)
	47.	A 2D crossover-based map of the human X chromosome as a model for map integration. [electronic resource] by Fain, P R Kort, E N Chance, P F Nguyen, K Redd, D F Econs, M J Barker, D F Producer: 19950712 In: Nature genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers. [electronic resource] by Lebo, R V Lynch, E D Bird, T D Golbus, M S Barker, D F O'Connell, P Chance, P F Producer: 19920213 In: American journal of human genetics vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	49.	Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome. [electronic resource] by Lafrenière, R G Brown, C J Powers, V E Carrel, L Davies, K E Barker, D F Willard, H F Producer: 19920221 In: Genomics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome? [electronic resource] by Stern, H J Saal, H M Lee, J S Fain, P R Goldgar, D E Rosenbaum, K N Barker, D F Producer: 19920428 In: Journal of medical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	MRX8: an X-linked mental retardation condition with linkage to Xq21. [electronic resource] by Schwartz, C E May, M Huang, T Ledbetter, D Anderson, G Barker, D F Lubs, H A Arena, F Stevenson, R E Producer: 19920716 In: American journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	52.	Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22. [electronic resource] by Parolini, O Hejtmancik, J F Allen, R C Belmont, J W Lassiter, G L Henry, M J Barker, D F Conley, M E Producer: 19930414 In: Genomics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	53.	BRCA1 R841W: a strong candidate for a common mutation with moderate phenotype. [electronic resource] by Barker, D F Almeida, E R Casey, G Fain, P R Liao, S Y Masunaka, I Noble, B Kurosaki, T Anton-Culver, H Producer: 19970306 In: Genetic epidemiology vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	54.	Genetic analysis of NF1: identification of close flanking markers on chromosome 17. [electronic resource] by Fain, P R Barker, D F Goldgar, D E Wright, E Nguyen, K Carey, J Johnson, J Kivlin, J Willard, H Mathew, C Producer: 19880616 In: Genomics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	55.	A mutation causing Alport syndrome with tardive hearing loss is common in the western United States. [electronic resource] by Barker, D F Pruchno, C J Jiang, X Atkin, C L Stone, E M Denison, J C Fain, P R Gregory, M C Producer: 19960725 In: American journal of human genetics vol. 58 Availability: No items available. Save to lists Add to cart (remove)
	56.	Paternal origin of new mutations in von Recklinghausen neurofibromatosis. [electronic resource] by Jadayel, D Fain, P Upadhyaya, M Ponder, M A Huson, S M Carey, J Fryer, A Mathew, C G Barker, D F Ponder, B A Producer: 19900313 In: Nature vol. 343 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	57.	Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group. [electronic resource] by Raeymaekers, P Timmerman, V Nelis, E De Jonghe, P Hoogendijk, J E Baas, F Barker, D F Martin, J J De Visser, M Bolhuis, P A Producer: 19920910 In: Neuromuscular disorders : NMD vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	58.	Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region. [electronic resource] by Ledbetter, D H Ledbetter, S A vanTuinen, P Summers, K M Robinson, T J Nakamura, Y Wolff, R White, R Barker, D F Wallace, M R Producer: 19890810 In: Proceedings of the National Academy of Sciences of the United States of America vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	59.	Identification of more than 500 RFLPs by screening random genomic clones. [electronic resource] by Schumm, J W Knowlton, R G Braman, J C Barker, D F Botstein, D Akots, G Brown, V A Gravius, T C Helms, C Hsiao, K Producer: 19880223 In: American journal of human genetics vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	60.	Fine structure mapping of the human X-linked hypophosphatemic rickets gene locus. [electronic resource] by Econs, M J Rowe, P S Francis, F Barker, D F Speer, M C Norman, M Fain, P R Weissenbach, J Read, A Davis, K E Producer: 19941221 In: The Journal of clinical endocrinology and metabolism vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search

Availability

Authors

Topics

Languages

Your search returned 71 results.