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D W Cox

Showing results (171-180 of 223) with videos related to

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Clinical Genetics|November 15, 2005
COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiologyV A Coronado, J A Bonneville, H Nazer, et al.
Genomics|March 15, 1997
Genetic polymorphism and recombination in the subtelomeric region of chromosome 14qR F Wintle, T G Nygaard, J A Herbrick, et al.
Genomics|January 1, 1990
Physical mapping of probes within 14q32, a subtelomeric region showing a high recombination frequencyM H Hofker, S Smith, Y Nakamura, et al.
Irish Medical Journal|September 20, 2019
The Prevalence of Pseudomonas Aeruginosa Infection Over a Ten-Year Period in Children with Cystic FibrosisK Al Shidhani, R O’Reilly, S Javadpour, et al.
Genomics|July 15, 1997
Physical and transcription map in the region 14q24.3: identification of six novel transcriptsA F Roux, J M Rommens, L Read, et al.
Nature Genetics|December 1, 1993
The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes geneP C Bull, G R Thomas, J M Rommens, et al.
The Journal of Clinical Investigation|December 1, 1990
A null deficiency allele of alpha 1-antitrypsin, QOludwigshafen, with altered tertiary structureG C Frazier, M A Siewertsen, M H Hofker, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|June 11, 2020
The role of rhinovirus infections in young children with cystic fibrosisD W O Loughlin, S Coughlan, C F De Gascun, et al.
American Journal of Human Genetics|January 1, 1994
Haplotype studies in Wilson diseaseG R Thomas, P C Bull, E A Roberts, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Regional localization of loci on chromosome 14 using somatic cell hybridsG D Billingsley, D W Cox, A M Duncan, et al.
Pageof 23

Showing results (171-180 of 223) with videos related to

Sort By:
Pageof 23
Clinical Genetics|November 15, 2005
COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiologyV A Coronado, J A Bonneville, H Nazer, et al.
Genomics|March 15, 1997
Genetic polymorphism and recombination in the subtelomeric region of chromosome 14qR F Wintle, T G Nygaard, J A Herbrick, et al.
Genomics|January 1, 1990
Physical mapping of probes within 14q32, a subtelomeric region showing a high recombination frequencyM H Hofker, S Smith, Y Nakamura, et al.
Irish Medical Journal|September 20, 2019
The Prevalence of Pseudomonas Aeruginosa Infection Over a Ten-Year Period in Children with Cystic FibrosisK Al Shidhani, R O’Reilly, S Javadpour, et al.
Genomics|July 15, 1997
Physical and transcription map in the region 14q24.3: identification of six novel transcriptsA F Roux, J M Rommens, L Read, et al.
Nature Genetics|December 1, 1993
The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes geneP C Bull, G R Thomas, J M Rommens, et al.
The Journal of Clinical Investigation|December 1, 1990
A null deficiency allele of alpha 1-antitrypsin, QOludwigshafen, with altered tertiary structureG C Frazier, M A Siewertsen, M H Hofker, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|June 11, 2020
The role of rhinovirus infections in young children with cystic fibrosisD W O Loughlin, S Coughlan, C F De Gascun, et al.
American Journal of Human Genetics|January 1, 1994
Haplotype studies in Wilson diseaseG R Thomas, P C Bull, E A Roberts, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Regional localization of loci on chromosome 14 using somatic cell hybridsG D Billingsley, D W Cox, A M Duncan, et al.
Pageof 23