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 J Lench

Showing results (11-20 of 39) with videos related to

Pageof 4
Sort By:
European Journal of Cancer. Part B, Oral Oncology|May 1, 1996
Investigation of chromosome 9q22.3-q31 DNA marker loss in odontogenic keratocystsN J Lench, A S High, A F Markham, et al.
Biochemical and Biophysical Research Communications|February 3, 1998
cDNA cloning, genomic organization, and chromosomal localization of a novel human gene that encodes a kinesin-related protein highly similar to mouse Kif3CE A Telford, P Wightman, J Leek, et al.
Cytogenetics and Cell Genetics|August 6, 1998
Detailed genetic mapping around a putative prostate-specific membrane antigen locus on human chromosome 11p11.2B H Maraj, J P Leek, M Karayi, et al.
Human Genetics|October 28, 1997
Characterisation of human patched germ line mutations in naevoid basal cell carcinoma syndromeN J Lench, E A Telford, A S High, et al.
Genomics|December 1, 1996
An EST and STS-based YAC contig map of human chromosome 9q22.3N J Lench, E A Telford, S E Andersen, et al.
Annals of Human Genetics|September 1, 1996
Human sequences homologous to the gene for the cochlear protein Ocp-II do not map to currently known non-syndromic hearing loss lociK A Brown, J P Leek, N J Lench, et al.
Journal of Medical Genetics|August 1, 1997
Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1K A Brown, L I al-Gazali, L M Moynihan, et al.
American Journal of Human Genetics|May 23, 1998
A syndrome of severe mental retardation, spasticity, and tapetoretinal degeneration linked to chromosome 15q24S J Mitchell, D P McHale, D A Campbell, et al.
Oral Diseases|October 5, 2002
Molecular analysis for genetic counselling in amelogenesis imperfectaM J Aldred, R K Hall, N Kilpatrick, et al.
Nature|May 1, 1997
Connexin 26 mutations in hereditary non-syndromic sensorineural deafnessD P Kelsell, J Dunlop, H P Stevens, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
European Journal of Cancer. Part B, Oral Oncology|May 1, 1996
Investigation of chromosome 9q22.3-q31 DNA marker loss in odontogenic keratocystsN J Lench, A S High, A F Markham, et al.
Biochemical and Biophysical Research Communications|February 3, 1998
cDNA cloning, genomic organization, and chromosomal localization of a novel human gene that encodes a kinesin-related protein highly similar to mouse Kif3CE A Telford, P Wightman, J Leek, et al.
Cytogenetics and Cell Genetics|August 6, 1998
Detailed genetic mapping around a putative prostate-specific membrane antigen locus on human chromosome 11p11.2B H Maraj, J P Leek, M Karayi, et al.
Human Genetics|October 28, 1997
Characterisation of human patched germ line mutations in naevoid basal cell carcinoma syndromeN J Lench, E A Telford, A S High, et al.
Genomics|December 1, 1996
An EST and STS-based YAC contig map of human chromosome 9q22.3N J Lench, E A Telford, S E Andersen, et al.
Annals of Human Genetics|September 1, 1996
Human sequences homologous to the gene for the cochlear protein Ocp-II do not map to currently known non-syndromic hearing loss lociK A Brown, J P Leek, N J Lench, et al.
Journal of Medical Genetics|August 1, 1997
Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1K A Brown, L I al-Gazali, L M Moynihan, et al.
American Journal of Human Genetics|May 23, 1998
A syndrome of severe mental retardation, spasticity, and tapetoretinal degeneration linked to chromosome 15q24S J Mitchell, D P McHale, D A Campbell, et al.
Oral Diseases|October 5, 2002
Molecular analysis for genetic counselling in amelogenesis imperfectaM J Aldred, R K Hall, N Kilpatrick, et al.
Nature|May 1, 1997
Connexin 26 mutations in hereditary non-syndromic sensorineural deafnessD P Kelsell, J Dunlop, H P Stevens, et al.
Pageof 4