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

J S Waye

Showing results (111-120 of 115) with videos related to

Pageof 12
Sort By:
You have reached the last page of results.This site can display upto 115 results.
American Journal of Human Genetics|May 1, 1991
Fixed-bin analysis for statistical evaluation of continuous distributions of allelic data from VNTR loci, for use in forensic comparisonsB Budowle, A M Giusti, J S Waye, et al.
Genetic Testing|September 12, 2001
Universal newborn screening for Hb H disease in CaliforniaF Lorey, G Cunningham, E P Vichinsky, et al.
British Journal of Haematology|November 1, 1995
The prenatal identification of fetal compatibility in neonatal alloimmune thrombocytopenia using amniotic fluid and variable number of tandem repeat (VNTR) analysisG A Denomme, J S Waye, R F Burrows, et al.
Journal of Medical Genetics|April 5, 2005
DHCR7 nonsense mutations and characterisation of mRNA nonsense mediated decay in Smith-Lemli-Opitz syndromeL S Correa-Cerro, C A Wassif, J S Waye, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effectsS W Horsley, R J Daniels, E Anguita, et al.
Pageof 12

Showing results (111-120 of 115) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 115 results.
American Journal of Human Genetics|May 1, 1991
Fixed-bin analysis for statistical evaluation of continuous distributions of allelic data from VNTR loci, for use in forensic comparisonsB Budowle, A M Giusti, J S Waye, et al.
Genetic Testing|September 12, 2001
Universal newborn screening for Hb H disease in CaliforniaF Lorey, G Cunningham, E P Vichinsky, et al.
British Journal of Haematology|November 1, 1995
The prenatal identification of fetal compatibility in neonatal alloimmune thrombocytopenia using amniotic fluid and variable number of tandem repeat (VNTR) analysisG A Denomme, J S Waye, R F Burrows, et al.
Journal of Medical Genetics|April 5, 2005
DHCR7 nonsense mutations and characterisation of mRNA nonsense mediated decay in Smith-Lemli-Opitz syndromeL S Correa-Cerro, C A Wassif, J S Waye, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effectsS W Horsley, R J Daniels, E Anguita, et al.
Pageof 12