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Protein Engineering
|
March 1, 1997
Improvement of thermal stability of Streptomyces cholesterol oxidase by random mutagenesis and a structural interpretation
Y Nishiya, N Harada, S I Teshima, et al.
American Journal of Medical Genetics
|
September 13, 2000
Analphoid 3qter markers
I 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 recombination
J 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 therapies
C 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 syndromes
I Teshima, D Chadwick, D Chitayat, et al.
American Journal of Medical Genetics
|
March 31, 1997
Omphalocele in Miller-Dieker syndrome: expanding the phenotype
D 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 imprinted
R Weksberg, I Teshima, B R Williams, et al.
Journal of Medical Genetics
|
October 3, 1999
Microdeletion 22q11.2: clinical data and deletion size
W S Kerstjens-Frederikse, H Kurahashi, D A Driscoll, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 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 interpretation
Y Nishiya, N Harada, S I Teshima, et al.
American Journal of Medical Genetics
|
September 13, 2000
Analphoid 3qter markers
I 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 recombination
J 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 therapies
C 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 syndromes
I Teshima, D Chadwick, D Chitayat, et al.
American Journal of Medical Genetics
|
March 31, 1997
Omphalocele in Miller-Dieker syndrome: expanding the phenotype
D 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 imprinted
R Weksberg, I Teshima, B R Williams, et al.
Journal of Medical Genetics
|
October 3, 1999
Microdeletion 22q11.2: clinical data and deletion size
W S Kerstjens-Frederikse, H Kurahashi, D A Driscoll, et al.
Page
of 3