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J R Lupski

Showing results (141-150 of 209) with videos related to

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Journal of Clinical Microbiology|December 1, 1994
Molecular fingerprinting of Legionella species by repetitive element PCRP R Georghiou, A M Doggett, M A Kielhofner, et al.
American Journal of Human Genetics|June 1, 1994
Detection of tandem duplications and implications for linkage analysisT C Matise, A Chakravarti, P I Patel, et al.
American Journal of Human Genetics|February 11, 1999
Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt diseaseR A Lewis, N F Shroyer, N Singh, et al.
American Journal of Medical Genetics|July 31, 2001
Defining the breakpoints of proximal chromosome 14q rearrangements in nine patients using flow-sorted chromosomesD Kamnasaran, P C O'Brien, S Schuffenhauer, et al.
American Journal of Human Genetics|December 1, 1999
Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigreesN Katsanis, R A Lewis, D W Stockton, et al.
Journal of Clinical Microbiology|August 1, 1995
Molecular genotyping of methicillin-resistant Staphylococcus aureus via fluorophore-enhanced repetitive-sequence PCRV G Del Vecchio, J M Petroziello, M J Gress, et al.
American Journal of Human Genetics|December 1, 1990
Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybridsP I Patel, C Garcia, R Montes de Oca-Luna, et al.
Journal of Medical Genetics|June 14, 2000
Circadian rhythm abnormalities of melatonin in Smith-Magenis syndromeL Potocki, D Glaze, D X Tan, et al.
Human Molecular Genetics|February 3, 2000
Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locusB A Bejjani, D W Stockton, R A Lewis, et al.
Genome Research|May 31, 2001
The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genesK Inoue, K Dewar, N Katsanis, et al.
Pageof 21

Showing results (141-150 of 209) with videos related to

Sort By:
Pageof 21
Journal of Clinical Microbiology|December 1, 1994
Molecular fingerprinting of Legionella species by repetitive element PCRP R Georghiou, A M Doggett, M A Kielhofner, et al.
American Journal of Human Genetics|June 1, 1994
Detection of tandem duplications and implications for linkage analysisT C Matise, A Chakravarti, P I Patel, et al.
American Journal of Human Genetics|February 11, 1999
Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt diseaseR A Lewis, N F Shroyer, N Singh, et al.
American Journal of Medical Genetics|July 31, 2001
Defining the breakpoints of proximal chromosome 14q rearrangements in nine patients using flow-sorted chromosomesD Kamnasaran, P C O'Brien, S Schuffenhauer, et al.
American Journal of Human Genetics|December 1, 1999
Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigreesN Katsanis, R A Lewis, D W Stockton, et al.
Journal of Clinical Microbiology|August 1, 1995
Molecular genotyping of methicillin-resistant Staphylococcus aureus via fluorophore-enhanced repetitive-sequence PCRV G Del Vecchio, J M Petroziello, M J Gress, et al.
American Journal of Human Genetics|December 1, 1990
Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybridsP I Patel, C Garcia, R Montes de Oca-Luna, et al.
Journal of Medical Genetics|June 14, 2000
Circadian rhythm abnormalities of melatonin in Smith-Magenis syndromeL Potocki, D Glaze, D X Tan, et al.
Human Molecular Genetics|February 3, 2000
Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locusB A Bejjani, D W Stockton, R A Lewis, et al.
Genome Research|May 31, 2001
The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genesK Inoue, K Dewar, N Katsanis, et al.
Pageof 21