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

S W Scherer

Showing results (121-130 of 164) with videos related to

Pageof 17
Sort By:
Human Molecular Genetics|July 1, 1997
Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndromeI Krebs, I Weis, M Hudler, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 18, 1998
Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuriaD Leclerc, A Wilson, R Dumas, et al.
Blood|December 3, 1998
Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disordersK Döhner, J Brown, U Hehmann, et al.
Journal of Medical Genetics|September 10, 2003
Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22E M Chan, D E Bulman, A D Paterson, et al.
Journal of Medical Genetics|April 5, 2003
The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndromeL Bentley, K Nakabayashi, D Monk, et al.
Oncogene|December 22, 1999
Dysregulation of cyclin dependent kinase 6 expression in splenic marginal zone lymphoma through chromosome 7q translocationsM M Corcoran, S J Mould, J A Orchard, et al.
Genomics|February 13, 2001
Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2S Hadano, Y Yanagisawa, J Skaug, et al.
Genomics|September 1, 1996
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patientsL R Osborne, D Martindale, S W Scherer, et al.
Clinical Genetics|March 30, 2010
Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from PakistanM A Rafiq, M Ansar, C R Marshall, et al.
Cell|August 23, 1996
MADR2 maps to 18q21 and encodes a TGFbeta-regulated MAD-related protein that is functionally mutated in colorectal carcinomaK Eppert, S W Scherer, H Ozcelik, et al.
Pageof 17

Showing results (121-130 of 164) with videos related to

Sort By:
Pageof 17
Human Molecular Genetics|July 1, 1997
Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndromeI Krebs, I Weis, M Hudler, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 18, 1998
Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuriaD Leclerc, A Wilson, R Dumas, et al.
Blood|December 3, 1998
Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disordersK Döhner, J Brown, U Hehmann, et al.
Journal of Medical Genetics|September 10, 2003
Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22E M Chan, D E Bulman, A D Paterson, et al.
Journal of Medical Genetics|April 5, 2003
The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndromeL Bentley, K Nakabayashi, D Monk, et al.
Oncogene|December 22, 1999
Dysregulation of cyclin dependent kinase 6 expression in splenic marginal zone lymphoma through chromosome 7q translocationsM M Corcoran, S J Mould, J A Orchard, et al.
Genomics|February 13, 2001
Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2S Hadano, Y Yanagisawa, J Skaug, et al.
Genomics|September 1, 1996
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patientsL R Osborne, D Martindale, S W Scherer, et al.
Clinical Genetics|March 30, 2010
Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from PakistanM A Rafiq, M Ansar, C R Marshall, et al.
Cell|August 23, 1996
MADR2 maps to 18q21 and encodes a TGFbeta-regulated MAD-related protein that is functionally mutated in colorectal carcinomaK Eppert, S W Scherer, H Ozcelik, et al.
Pageof 17