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

L D Keppen

Showing results (11-20 of 18) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 18 results.
Neurotoxicology|January 1, 1988
Autism in association with fragile X syndrome in females: implications for diagnosis and treatment in childrenD R Edwards, L D Keppen, J D Ranells, et al.
American Journal of Ophthalmology|April 15, 1990
Ocular and systemic findings in the Aarskog (facial-digital-genital) syndromeM C Brodsky, L D Keppen, C D Rice, et al.
American Journal of Medical Genetics|October 1, 1992
Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5L D Keppen, S M Gollin, D Edwards, et al.
American Journal of Medical Genetics|March 3, 1997
New syndrome of spondylospinal thoracic dysostosis with multiple pterygia and arthrogryposisV P Johnson, L D Keppen, M S Carpenter, et al.
Neurology|April 1, 1996
Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegiaF Cambi, X M Tang, P Cordray, et al.
Clinical Genetics|December 8, 1998
Prenatal diagnosis of a trisomy 17p derived from a de novo non-mosaic satellited markerA S Kulharya, J Garcia-Heras, H B Radtke, et al.
The Journal of Pediatrics|September 1, 1988
Confirmation of autosomal dominant transmission of the DiGeorge malformation complexL D Keppen, J W Fasules, A W Burks, et al.
American Journal of Human Genetics|November 1, 1987
Etiological heterogeneity in X-linked spastic paraplegiaL D Keppen, M F Leppert, P O'Connell, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Neurotoxicology|January 1, 1988
Autism in association with fragile X syndrome in females: implications for diagnosis and treatment in childrenD R Edwards, L D Keppen, J D Ranells, et al.
American Journal of Ophthalmology|April 15, 1990
Ocular and systemic findings in the Aarskog (facial-digital-genital) syndromeM C Brodsky, L D Keppen, C D Rice, et al.
American Journal of Medical Genetics|October 1, 1992
Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5L D Keppen, S M Gollin, D Edwards, et al.
American Journal of Medical Genetics|March 3, 1997
New syndrome of spondylospinal thoracic dysostosis with multiple pterygia and arthrogryposisV P Johnson, L D Keppen, M S Carpenter, et al.
Neurology|April 1, 1996
Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegiaF Cambi, X M Tang, P Cordray, et al.
Clinical Genetics|December 8, 1998
Prenatal diagnosis of a trisomy 17p derived from a de novo non-mosaic satellited markerA S Kulharya, J Garcia-Heras, H B Radtke, et al.
The Journal of Pediatrics|September 1, 1988
Confirmation of autosomal dominant transmission of the DiGeorge malformation complexL D Keppen, J W Fasules, A W Burks, et al.
American Journal of Human Genetics|November 1, 1987
Etiological heterogeneity in X-linked spastic paraplegiaL D Keppen, M F Leppert, P O'Connell, et al.
Pageof 2