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

T E Kelly

Showing results (51-60 of 103) with videos related to

Pageof 11
Sort By:
Lancet (London, England)|November 10, 1973
Letter: Screening for mucolipidosisT E Kelly, G H Thomas, H A Taylor
Birth Defects Original Article Series|January 1, 1977
An unusual familial spondyloepiphyseal dysplasia: "spondyloperipheral dysplasia"T E Kelly, J R Lichtenstein, J P Dorst
American Journal of Human Genetics|January 1, 1981
A possible exception to the critical region hypothesisV M Barnabei, H E Wyandt, T E Kelly
Clinical Genetics|May 1, 1976
Segregation within a family of two mutant alleles for hexosaminidase AT E Kelly, L W Reynolds, J S O'Brien
Clinical Cardiology|May 1, 1991
Progression of cardiac disease in Emery-Dreifuss muscular dystrophyM G Bialer, N L McDaniel, T E Kelly
American Journal of Medical Genetics|July 1, 1989
Apparent Ruvalcaba syndrome with genitourinary abnormalitiesM G Bialer, W G Wilson, T E Kelly
American Journal of Medical Genetics|January 1, 1985
De novo 21q interstitial deletion in a retarded boy with ulno-fibular dysostosisJ F Reynolds, H E Wyandt, T E Kelly
American Journal of Medical Genetics|January 1, 1982
The Weissenbacher-Zweymüller syndrome: possible neonatal expression of the Stickler syndromeT E Kelly, H H Wells, K B Tuck
Neurology|April 1, 1985
Hereditary motor-sensory neuropathy (HMSN): possible X-linked dominant inheritanceL H Phillips, T E Kelly, P Schnatterly, et al.
Prenatal Diagnosis|December 17, 1998
Confined placental mosaicism for trisomy 8 and intra-uterine growth retardationE Saks, M C Mccoy, J Damron, et al.
Pageof 11

Showing results (51-60 of 103) with videos related to

Sort By:
Pageof 11
Lancet (London, England)|November 10, 1973
Letter: Screening for mucolipidosisT E Kelly, G H Thomas, H A Taylor
Birth Defects Original Article Series|January 1, 1977
An unusual familial spondyloepiphyseal dysplasia: "spondyloperipheral dysplasia"T E Kelly, J R Lichtenstein, J P Dorst
American Journal of Human Genetics|January 1, 1981
A possible exception to the critical region hypothesisV M Barnabei, H E Wyandt, T E Kelly
Clinical Genetics|May 1, 1976
Segregation within a family of two mutant alleles for hexosaminidase AT E Kelly, L W Reynolds, J S O'Brien
Clinical Cardiology|May 1, 1991
Progression of cardiac disease in Emery-Dreifuss muscular dystrophyM G Bialer, N L McDaniel, T E Kelly
American Journal of Medical Genetics|July 1, 1989
Apparent Ruvalcaba syndrome with genitourinary abnormalitiesM G Bialer, W G Wilson, T E Kelly
American Journal of Medical Genetics|January 1, 1985
De novo 21q interstitial deletion in a retarded boy with ulno-fibular dysostosisJ F Reynolds, H E Wyandt, T E Kelly
American Journal of Medical Genetics|January 1, 1982
The Weissenbacher-Zweymüller syndrome: possible neonatal expression of the Stickler syndromeT E Kelly, H H Wells, K B Tuck
Neurology|April 1, 1985
Hereditary motor-sensory neuropathy (HMSN): possible X-linked dominant inheritanceL H Phillips, T E Kelly, P Schnatterly, et al.
Prenatal Diagnosis|December 17, 1998
Confined placental mosaicism for trisomy 8 and intra-uterine growth retardationE Saks, M C Mccoy, J Damron, et al.
Pageof 11