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

J Aldred

Showing results (101-110 of 105) with videos related to

Pageof 11
Sort By:
You have reached the last page of results.This site can display upto 105 results.
Connective Tissue Research|September 4, 2003
Relationship of phenotype and genotype in X-linked amelogenesis imperfectaJ T Wright, P S Hart, M J Aldred, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregateLouise M Downey, T Jeffrey Keen, Ismail K Jalili, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|March 18, 2026
Golden Jubilee of the International Association of Oral and Maxillofacial Pathologists (IAOP)Pablo A Vargas, Alan R Santos-Silva, Mark W Lingen, et al.
Pathology|October 14, 2003
Oral focal mucinosis: report of 15 cases and review of the literatureMichael J Aldred, Anna A Talacko, Kevin Ruljancich, et al.
American Journal of Human Genetics|August 21, 2012
Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfectaDavid A Parry, Steven J Brookes, Clare V Logan, et al.
Pageof 11

Showing results (101-110 of 105) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 105 results.
Connective Tissue Research|September 4, 2003
Relationship of phenotype and genotype in X-linked amelogenesis imperfectaJ T Wright, P S Hart, M J Aldred, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregateLouise M Downey, T Jeffrey Keen, Ismail K Jalili, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|March 18, 2026
Golden Jubilee of the International Association of Oral and Maxillofacial Pathologists (IAOP)Pablo A Vargas, Alan R Santos-Silva, Mark W Lingen, et al.
Pathology|October 14, 2003
Oral focal mucinosis: report of 15 cases and review of the literatureMichael J Aldred, Anna A Talacko, Kevin Ruljancich, et al.
American Journal of Human Genetics|August 21, 2012
Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfectaDavid A Parry, Steven J Brookes, Clare V Logan, et al.
Pageof 11