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

S E Mole

Showing results (31-40 of 54) with videos related to

Pageof 6
Sort By:
Ophthalmic Genetics|August 1, 2000
Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 geneL B Eksandh, V B Ponjavic, P B Munroe, et al.
American Journal of Medical Genetics|June 5, 1995
Phenol sulfotransferases: candidate genes for Batten diseaseT P Dooley, P Probst, R D Obermoeller, et al.
Journal of Medical Genetics|September 11, 1998
Sharing of PPT mutations between distinct clinical forms of neuronal ceroid lipofuscinoses in patients from ScotlandP B Munroe, N D Greene, K Y Leung, et al.
American Journal of Medical Genetics|June 5, 1995
Physical map of the region containing the gene for Batten disease (CLN3)I E Järvelä, H M Mitchison, D F Callen, et al.
Neurology|January 31, 2007
Adult neuronal ceroid lipofuscinosis caused by deficiency in palmitoyl protein thioesterase 1H Ramadan, A S Al-Din, A Ismail, et al.
Human Genetics|March 1, 1994
A multiple interval physical map of the pericentromeric region of human chromosome 10A Tunnacliffe, M S Jackson, E Gardner, et al.
Neuropediatrics|February 1, 1997
Strategy for mutation detection in CLN3: characterisation of two Finnish mutationsP B Munroe, A M O'Rawe, H M Mitchison, et al.
Human Molecular Genetics|March 1, 1993
Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2E Gardner, L Papi, D F Easton, et al.
American Journal of Human Genetics|March 1, 1995
Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease)P E Taschner, N de Vos, A D Thompson, et al.
Current Pharmaceutical Biotechnology|January 18, 2011
Therapeutic approaches to the challenge of neuronal ceroid lipofuscinosesR Kohan, I A Cismondi, A M Oller-Ramirez, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
Ophthalmic Genetics|August 1, 2000
Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 geneL B Eksandh, V B Ponjavic, P B Munroe, et al.
American Journal of Medical Genetics|June 5, 1995
Phenol sulfotransferases: candidate genes for Batten diseaseT P Dooley, P Probst, R D Obermoeller, et al.
Journal of Medical Genetics|September 11, 1998
Sharing of PPT mutations between distinct clinical forms of neuronal ceroid lipofuscinoses in patients from ScotlandP B Munroe, N D Greene, K Y Leung, et al.
American Journal of Medical Genetics|June 5, 1995
Physical map of the region containing the gene for Batten disease (CLN3)I E Järvelä, H M Mitchison, D F Callen, et al.
Neurology|January 31, 2007
Adult neuronal ceroid lipofuscinosis caused by deficiency in palmitoyl protein thioesterase 1H Ramadan, A S Al-Din, A Ismail, et al.
Human Genetics|March 1, 1994
A multiple interval physical map of the pericentromeric region of human chromosome 10A Tunnacliffe, M S Jackson, E Gardner, et al.
Neuropediatrics|February 1, 1997
Strategy for mutation detection in CLN3: characterisation of two Finnish mutationsP B Munroe, A M O'Rawe, H M Mitchison, et al.
Human Molecular Genetics|March 1, 1993
Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2E Gardner, L Papi, D F Easton, et al.
American Journal of Human Genetics|March 1, 1995
Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease)P E Taschner, N de Vos, A D Thompson, et al.
Current Pharmaceutical Biotechnology|January 18, 2011
Therapeutic approaches to the challenge of neuronal ceroid lipofuscinosesR Kohan, I A Cismondi, A M Oller-Ramirez, et al.
Pageof 6