Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

K Cowell

Showing results (51-60 of 266) with videos related to

Pageof 27
Sort By:
British Journal of Cancer|May 1, 1992
Follow-up of retinoblastoma patients having prenatal and perinatal predictions for mutant gene carrier status using intragenic polymorphic probes from the RB1 geneZ Onadim, J Hungerford, J K Cowell
British Journal of Cancer|November 1, 1993
Mechanisms of oncogenesis in patients with familial retinoblastomaZ Onadim, A Hogg, J K Cowell
Genesis (New York, N.Y. : 2000)|November 30, 2018
Selective inactivation of LGI1 in neuronal precursor cells leads to cortical dysplasia in miceJeane Silva, Haiyan Qin, John K Cowell
Brain Pathology (Zurich, Switzerland)|October 28, 2014
Homozygous Deletion of the LGI1 Gene in Mice Leads to Developmental Abnormalities Resulting in Cortical DysplasiaJeane Silva, Suash Sharma, John K Cowell
Human Molecular Genetics|June 9, 1998
NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastomaT Roberts, O Chernova, J K Cowell
Archives of Disease in Childhood|January 1, 1987
The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletionsJ K Cowell, E Thompson, P Rutland
Cancer Genetics and Cytogenetics|December 24, 1997
Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21)T Roberts, O Chernova, J K Cowell
Genomics|September 1, 1996
Regional localization of 192 genic markers on human chromosome 1T Roberts, C Auffray, J K Cowell
European Journal of Human Genetics : EJHG|January 1, 1994
Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastomaJ K Cowell, T Smith, B Bia
Cancer Genetics and Cytogenetics|September 1, 1988
Cytogenetic changes in Wilms' tumorsV Solis, J Pritchard, J K Cowell
Pageof 27

Showing results (51-60 of 266) with videos related to

Sort By:
Pageof 27
British Journal of Cancer|May 1, 1992
Follow-up of retinoblastoma patients having prenatal and perinatal predictions for mutant gene carrier status using intragenic polymorphic probes from the RB1 geneZ Onadim, J Hungerford, J K Cowell
British Journal of Cancer|November 1, 1993
Mechanisms of oncogenesis in patients with familial retinoblastomaZ Onadim, A Hogg, J K Cowell
Genesis (New York, N.Y. : 2000)|November 30, 2018
Selective inactivation of LGI1 in neuronal precursor cells leads to cortical dysplasia in miceJeane Silva, Haiyan Qin, John K Cowell
Brain Pathology (Zurich, Switzerland)|October 28, 2014
Homozygous Deletion of the LGI1 Gene in Mice Leads to Developmental Abnormalities Resulting in Cortical DysplasiaJeane Silva, Suash Sharma, John K Cowell
Human Molecular Genetics|June 9, 1998
NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastomaT Roberts, O Chernova, J K Cowell
Archives of Disease in Childhood|January 1, 1987
The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletionsJ K Cowell, E Thompson, P Rutland
Cancer Genetics and Cytogenetics|December 24, 1997
Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21)T Roberts, O Chernova, J K Cowell
Genomics|September 1, 1996
Regional localization of 192 genic markers on human chromosome 1T Roberts, C Auffray, J K Cowell
European Journal of Human Genetics : EJHG|January 1, 1994
Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastomaJ K Cowell, T Smith, B Bia
Cancer Genetics and Cytogenetics|September 1, 1988
Cytogenetic changes in Wilms' tumorsV Solis, J Pritchard, J K Cowell
Pageof 27