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

A O Wilkie

Showing results (1-10 of 82) with videos related to

Pageof 9
Sort By:
Journal of Medical Genetics|February 1, 1994
The molecular basis of genetic dominanceA O Wilkie
American Journal of Human Genetics|September 1, 1993
Detection of cryptic chromosomal abnormalities in unexplained mental retardation: a general strategy using hypervariable subtelomeric DNA polymorphismsA O Wilkie
American Journal of Medical Genetics|December 22, 1999
Epidemiology and genetics of craniosynostosisA O Wilkie
American Journal of Human Genetics|February 1, 1993
Errors in human gene mapping 11A O Wilkie
Indian Journal of Pediatrics|May 1, 1996
Fibroblast growth factor receptor mutations and craniosynostosis: three receptors, five syndromesA O Wilkie
Human Molecular Genetics|January 1, 1997
Craniosynostosis: genes and mechanismsA O Wilkie
British Medical Bulletin|July 1, 1996
The genetics of mental retardationJ Flint, A O Wilkie
Journal of Craniofacial Genetics and Developmental Biology|December 2, 2000
Pfeiffer syndrome is not caused by haploinsufficient mutations of FGFR2D Johnson, A O Wilkie
Genomics|May 1, 1992
An unusually large (CA)n repeat in the region of divergence between subtelomeric alleles of human chromosome 16pA O Wilkie, D R Higgs
Human Genetics|October 30, 1999
Characterisation of the human snail (SNAI1) gene and exclusion as a major disease gene in craniosynostosisS R Twigg, A O Wilkie
Pageof 9

Showing results (1-10 of 82) with videos related to

Sort By:
Pageof 9
Journal of Medical Genetics|February 1, 1994
The molecular basis of genetic dominanceA O Wilkie
American Journal of Human Genetics|September 1, 1993
Detection of cryptic chromosomal abnormalities in unexplained mental retardation: a general strategy using hypervariable subtelomeric DNA polymorphismsA O Wilkie
American Journal of Medical Genetics|December 22, 1999
Epidemiology and genetics of craniosynostosisA O Wilkie
American Journal of Human Genetics|February 1, 1993
Errors in human gene mapping 11A O Wilkie
Indian Journal of Pediatrics|May 1, 1996
Fibroblast growth factor receptor mutations and craniosynostosis: three receptors, five syndromesA O Wilkie
Human Molecular Genetics|January 1, 1997
Craniosynostosis: genes and mechanismsA O Wilkie
British Medical Bulletin|July 1, 1996
The genetics of mental retardationJ Flint, A O Wilkie
Journal of Craniofacial Genetics and Developmental Biology|December 2, 2000
Pfeiffer syndrome is not caused by haploinsufficient mutations of FGFR2D Johnson, A O Wilkie
Genomics|May 1, 1992
An unusually large (CA)n repeat in the region of divergence between subtelomeric alleles of human chromosome 16pA O Wilkie, D R Higgs
Human Genetics|October 30, 1999
Characterisation of the human snail (SNAI1) gene and exclusion as a major disease gene in craniosynostosisS R Twigg, A O Wilkie
Pageof 9