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P J Wilson

Showing results (61-70 of 85) with videos related to

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Birth Defects Original Article Series|January 1, 1984
Characteristics of parental response to fetal alcohol syndromeP J Wilson, R V Scott, F H Briggs, et al.
Journal of the American Veterinary Medical Association|February 15, 1994
Epizootic canine rabies transmitted by coyotes in south TexasK A Clark, S U Neill, J S Smith, et al.
Birth Defects Original Article Series|January 1, 1984
A tool for the assessment and achievement of family goals within the clinical genetics serviceR V Scott, F H Briggs, P J Wilson, et al.
Bone Marrow Transplantation|January 1, 1990
The use of polymerase chain reaction (PCR) gene amplification and synthetic oligonucleotide probes for HLA-DP typing in bone marrow transplantationW M Howell, P R Evans, D A Sage, et al.
Lasers in Surgery and Medicine|January 1, 1996
Anisotropy of radiance in tissue phantoms and Dunning R3327 rat tumors: radiance measurements with flat cleaved fiber probesA M Ballangrud, P J Wilson, K Brown, et al.
Oncogene|October 9, 1998
Frequent loss of heterozygosity and three critical regions on the short arm of chromosome 8 in ovarian adenocarcinomasK Wright, P J Wilson, J Kerr, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1990
Hunter syndrome: isolation of an iduronate-2-sulfatase cDNA clone and analysis of patient DNAP J Wilson, C P Morris, D S Anson, et al.
Human Genetics|June 1, 1991
The clinical phenotype of two patients with a complete deletion of the iduronate-2-sulphatase gene (mucopolysaccharidosis II--Hunter syndrome)J E Wraith, A Cooper, M Thornley, et al.
Human Mutation|January 1, 1993
Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase geneJ J Hopwood, S Bunge, C P Morris, et al.
Human Molecular Genetics|February 1, 1996
Novel mutations detected in the TSC2 gene from both sporadic and familial TSC patientsP J Wilson, V Ramesh, A Kristiansen, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
Birth Defects Original Article Series|January 1, 1984
Characteristics of parental response to fetal alcohol syndromeP J Wilson, R V Scott, F H Briggs, et al.
Journal of the American Veterinary Medical Association|February 15, 1994
Epizootic canine rabies transmitted by coyotes in south TexasK A Clark, S U Neill, J S Smith, et al.
Birth Defects Original Article Series|January 1, 1984
A tool for the assessment and achievement of family goals within the clinical genetics serviceR V Scott, F H Briggs, P J Wilson, et al.
Bone Marrow Transplantation|January 1, 1990
The use of polymerase chain reaction (PCR) gene amplification and synthetic oligonucleotide probes for HLA-DP typing in bone marrow transplantationW M Howell, P R Evans, D A Sage, et al.
Lasers in Surgery and Medicine|January 1, 1996
Anisotropy of radiance in tissue phantoms and Dunning R3327 rat tumors: radiance measurements with flat cleaved fiber probesA M Ballangrud, P J Wilson, K Brown, et al.
Oncogene|October 9, 1998
Frequent loss of heterozygosity and three critical regions on the short arm of chromosome 8 in ovarian adenocarcinomasK Wright, P J Wilson, J Kerr, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1990
Hunter syndrome: isolation of an iduronate-2-sulfatase cDNA clone and analysis of patient DNAP J Wilson, C P Morris, D S Anson, et al.
Human Genetics|June 1, 1991
The clinical phenotype of two patients with a complete deletion of the iduronate-2-sulphatase gene (mucopolysaccharidosis II--Hunter syndrome)J E Wraith, A Cooper, M Thornley, et al.
Human Mutation|January 1, 1993
Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase geneJ J Hopwood, S Bunge, C P Morris, et al.
Human Molecular Genetics|February 1, 1996
Novel mutations detected in the TSC2 gene from both sporadic and familial TSC patientsP J Wilson, V Ramesh, A Kristiansen, et al.
Pageof 9