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

G E Houck

Showing results (11-20 of 19) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 19 results.
Clinical Genetics|September 11, 1992
Reassessment of a chromosome 12q+ marker by fluorescent in situ hybridization (FISH)A Jeziorowska, G E Houck, X L Yao, et al.
Journal of Genetic Counseling|November 16, 2013
Molecular carrier testing for the fragile X syndrome: Issues for genetic counselorsJ L Berliner, F N Shapiro, S L Nolin, et al.
American Journal of Medical Genetics|April 1, 1993
Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-->q31.3)A Jeziorowska, W Ciesla, G E Houck, et al.
JAMA|October 6, 1993
Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR testW T Brown, G E Houck, A Jeziorowska, et al.
American Journal of Medical Genetics|July 15, 1994
Fragile X induction systems in CVS cultures: effect on cytogenetic, PCR, and genomic Southern Blot DNA analyses of the FMR-1 geneE C Jenkins, I Morys, J Henderson, et al.
Biochemical and Biophysical Research Communications|February 29, 1988
Fine mapping of an Alzheimer disease-associated gene encoding beta-amyloid proteinE C Jenkins, E A Devine-Gage, N K Robakis, et al.
Progress in Clinical and Biological Research|January 1, 1989
Beta-amyloid protein probe hybridized to chromosome 9 in 3 Alzheimer disease individualsE C Jenkins, E A Devine-Gage, X L Yao, et al.
American Journal of Human Genetics|December 1, 1996
Familial transmission of the FMR1 CGG repeatS L Nolin, F A Lewis, L L Ye, et al.
American Journal of Medical Genetics|April 20, 1999
Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodiesE C Jenkins, G Y Wen, K S Kim, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Clinical Genetics|September 11, 1992
Reassessment of a chromosome 12q+ marker by fluorescent in situ hybridization (FISH)A Jeziorowska, G E Houck, X L Yao, et al.
Journal of Genetic Counseling|November 16, 2013
Molecular carrier testing for the fragile X syndrome: Issues for genetic counselorsJ L Berliner, F N Shapiro, S L Nolin, et al.
American Journal of Medical Genetics|April 1, 1993
Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-->q31.3)A Jeziorowska, W Ciesla, G E Houck, et al.
JAMA|October 6, 1993
Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR testW T Brown, G E Houck, A Jeziorowska, et al.
American Journal of Medical Genetics|July 15, 1994
Fragile X induction systems in CVS cultures: effect on cytogenetic, PCR, and genomic Southern Blot DNA analyses of the FMR-1 geneE C Jenkins, I Morys, J Henderson, et al.
Biochemical and Biophysical Research Communications|February 29, 1988
Fine mapping of an Alzheimer disease-associated gene encoding beta-amyloid proteinE C Jenkins, E A Devine-Gage, N K Robakis, et al.
Progress in Clinical and Biological Research|January 1, 1989
Beta-amyloid protein probe hybridized to chromosome 9 in 3 Alzheimer disease individualsE C Jenkins, E A Devine-Gage, X L Yao, et al.
American Journal of Human Genetics|December 1, 1996
Familial transmission of the FMR1 CGG repeatS L Nolin, F A Lewis, L L Ye, et al.
American Journal of Medical Genetics|April 20, 1999
Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodiesE C Jenkins, G Y Wen, K S Kim, et al.
Pageof 2