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I Teshima

Showing results (21-30 of 28) with videos related to

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Protein Engineering|March 1, 1997
Improvement of thermal stability of Streptomyces cholesterol oxidase by random mutagenesis and a structural interpretationY Nishiya, N Harada, S I Teshima, et al.
American Journal of Medical Genetics|September 13, 2000
Analphoid 3qter markersI Teshima, E V Bawle, R Weksberg, et al.
Genomics|April 1, 1991
Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: identification of a hot spot for recombinationJ C Benger, I Teshima, M A Walter, et al.
Pediatric Neurosurgery|March 7, 2000
Primary Ewing's sarcoma of the skull in children. Utility of molecular diagnostics, surgery and adjuvant therapiesC G Carlotti, J M Drake, J P Hladky, et al.
American Journal of Medical Genetics|March 29, 1996
FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromesI Teshima, D Chadwick, D Chitayat, et al.
American Journal of Medical Genetics|March 31, 1997
Omphalocele in Miller-Dieker syndrome: expanding the phenotypeD Chitayat, A Toi, R Babul, et al.
Human Molecular Genetics|May 1, 1993
Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprintedR Weksberg, I Teshima, B R Williams, et al.
Journal of Medical Genetics|October 3, 1999
Microdeletion 22q11.2: clinical data and deletion sizeW S Kerstjens-Frederikse, H Kurahashi, D A Driscoll, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Protein Engineering|March 1, 1997
Improvement of thermal stability of Streptomyces cholesterol oxidase by random mutagenesis and a structural interpretationY Nishiya, N Harada, S I Teshima, et al.
American Journal of Medical Genetics|September 13, 2000
Analphoid 3qter markersI Teshima, E V Bawle, R Weksberg, et al.
Genomics|April 1, 1991
Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: identification of a hot spot for recombinationJ C Benger, I Teshima, M A Walter, et al.
Pediatric Neurosurgery|March 7, 2000
Primary Ewing's sarcoma of the skull in children. Utility of molecular diagnostics, surgery and adjuvant therapiesC G Carlotti, J M Drake, J P Hladky, et al.
American Journal of Medical Genetics|March 29, 1996
FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromesI Teshima, D Chadwick, D Chitayat, et al.
American Journal of Medical Genetics|March 31, 1997
Omphalocele in Miller-Dieker syndrome: expanding the phenotypeD Chitayat, A Toi, R Babul, et al.
Human Molecular Genetics|May 1, 1993
Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprintedR Weksberg, I Teshima, B R Williams, et al.
Journal of Medical Genetics|October 3, 1999
Microdeletion 22q11.2: clinical data and deletion sizeW S Kerstjens-Frederikse, H Kurahashi, D A Driscoll, et al.
Pageof 3