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 Temple

Showing results (41-50 of 262) with videos related to

Pageof 27
Sort By:
The Journal of Experimental Biology|November 24, 2001
Embryonic temperature and the relative timing of muscle-specific genes during development in herring (Clupea harengus L.)G K Temple, N J Cole, I A Johnston
Archives of Disease in Childhood|September 1, 1990
The iris in Williams syndromeG Holmström, G Almond, K Temple, et al.
American Journal of Medical Genetics|July 23, 1998
Molecular confirmation of germ line mosaicism for a submicroscopic deletion of chromosome 22q11E Hatchwell, F Long, J Wilde, et al.
Diseases of the Colon and Rectum|October 10, 2012
Rectal cancer patients' quality of life with a temporary stoma: shifting perspectivesHeather B Neuman, Jason Park, Sarah Fuzesi, et al.
Journal of Medical Genetics|June 1, 1989
Dominantly inherited cleft lip and palate in two familiesK Temple, M Calvert, D Plint, et al.
Journal of Medical Genetics|February 1, 1991
Pitfalls in counselling: the craniosynostosesR Marini, K Temple, L Chitty, et al.
Journal of Medical Genetics|March 1, 1990
Focal dermal hypoplasia (Goltz syndrome)I K Temple, P MacDowall, M Baraitser, et al.
American Journal of Medical Genetics|September 1, 1990
Midline facial defects with ocular colobomataI K Temple, H Brunner, B Jones, et al.
Journal of Medical Genetics|May 29, 2007
Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriersK L Lachlan, A M Lucassen, D Bunyan, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
Leigh syndrome resulting from de novo mutation at position 8993 of mitochondrial DNAA Seller, C R Kennedy, I K Temple, et al.
Pageof 27

Showing results (41-50 of 262) with videos related to

Sort By:
Pageof 27
The Journal of Experimental Biology|November 24, 2001
Embryonic temperature and the relative timing of muscle-specific genes during development in herring (Clupea harengus L.)G K Temple, N J Cole, I A Johnston
Archives of Disease in Childhood|September 1, 1990
The iris in Williams syndromeG Holmström, G Almond, K Temple, et al.
American Journal of Medical Genetics|July 23, 1998
Molecular confirmation of germ line mosaicism for a submicroscopic deletion of chromosome 22q11E Hatchwell, F Long, J Wilde, et al.
Diseases of the Colon and Rectum|October 10, 2012
Rectal cancer patients' quality of life with a temporary stoma: shifting perspectivesHeather B Neuman, Jason Park, Sarah Fuzesi, et al.
Journal of Medical Genetics|June 1, 1989
Dominantly inherited cleft lip and palate in two familiesK Temple, M Calvert, D Plint, et al.
Journal of Medical Genetics|February 1, 1991
Pitfalls in counselling: the craniosynostosesR Marini, K Temple, L Chitty, et al.
Journal of Medical Genetics|March 1, 1990
Focal dermal hypoplasia (Goltz syndrome)I K Temple, P MacDowall, M Baraitser, et al.
American Journal of Medical Genetics|September 1, 1990
Midline facial defects with ocular colobomataI K Temple, H Brunner, B Jones, et al.
Journal of Medical Genetics|May 29, 2007
Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriersK L Lachlan, A M Lucassen, D Bunyan, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
Leigh syndrome resulting from de novo mutation at position 8993 of mitochondrial DNAA Seller, C R Kennedy, I K Temple, et al.
Pageof 27