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

N R Dennis

Showing results (11-20 of 66) with videos related to

Pageof 7
Sort By:
American Journal of Medical Genetics|August 15, 1994
Axial mesodermal dysplasia spectrum: affected sisters with oculoauriculovertebral "dysplasia" and caudal "regression" sequenceN R Dennis, J D Atwell
Journal of Medical Genetics|September 1, 1990
Deletion Xp22.3I K Temple, N R Dennis
American Journal of Medical Genetics|December 4, 1995
Lethal syndrome of slender bones, intrauterine fractures, characteristics facial appearance, and cataracts, resembling Hallermann-Streiff syndrome in two sibsN R Dennis, J Fairhurst, I E Moore
British Heart Journal|July 1, 1991
Familial Ebstein's anomaly: a report of six cases in two generations associated with mild skeletal abnormalitiesS Balaji, N R Dennis, B R Keeton
Archives of Disease in Childhood|December 1, 1973
Oesophageal atresia. 3 cases in 2 generationsN R Dennis, J L Nicholas, I Kovar
Journal of Medical Genetics|February 1, 1989
Interstitial deletion of distal 13q associated with Hirschsprung's diseaseM A Lamont, M Fitchett, N R Dennis
Clinical Genetics|January 1, 1987
Carrier detection in DMDG Uppal, K C Dewbury, N R Dennis
The British Journal of Radiology|April 1, 1981
Osteopathia striata with sclerosis and thickening of the skullM R Paling, I Hyde, N R Dennis
Archives of Disease in Childhood|March 1, 1986
Chromosome abnormalities in pupils attending ESN/M schoolsM A Lamont, N R Dennis, M Seabright
American Journal of Medical Genetics|January 1, 1978
Duplication 2q33 leads to 2q37 due to paternal ins (12;2) translocationN R Dennis, R L Neu, R M Bannerman
Pageof 7

Showing results (11-20 of 66) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics|August 15, 1994
Axial mesodermal dysplasia spectrum: affected sisters with oculoauriculovertebral "dysplasia" and caudal "regression" sequenceN R Dennis, J D Atwell
Journal of Medical Genetics|September 1, 1990
Deletion Xp22.3I K Temple, N R Dennis
American Journal of Medical Genetics|December 4, 1995
Lethal syndrome of slender bones, intrauterine fractures, characteristics facial appearance, and cataracts, resembling Hallermann-Streiff syndrome in two sibsN R Dennis, J Fairhurst, I E Moore
British Heart Journal|July 1, 1991
Familial Ebstein's anomaly: a report of six cases in two generations associated with mild skeletal abnormalitiesS Balaji, N R Dennis, B R Keeton
Archives of Disease in Childhood|December 1, 1973
Oesophageal atresia. 3 cases in 2 generationsN R Dennis, J L Nicholas, I Kovar
Journal of Medical Genetics|February 1, 1989
Interstitial deletion of distal 13q associated with Hirschsprung's diseaseM A Lamont, M Fitchett, N R Dennis
Clinical Genetics|January 1, 1987
Carrier detection in DMDG Uppal, K C Dewbury, N R Dennis
The British Journal of Radiology|April 1, 1981
Osteopathia striata with sclerosis and thickening of the skullM R Paling, I Hyde, N R Dennis
Archives of Disease in Childhood|March 1, 1986
Chromosome abnormalities in pupils attending ESN/M schoolsM A Lamont, N R Dennis, M Seabright
American Journal of Medical Genetics|January 1, 1978
Duplication 2q33 leads to 2q37 due to paternal ins (12;2) translocationN R Dennis, R L Neu, R M Bannerman
Pageof 7