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

C A Francomano

Showing results (11-20 of 101) with videos related to

Pageof 11
Sort By:
Current Opinion in Genetics & Development|June 1, 1996
Bone dysplasias in man: molecular insightsC A Francomano, I McIntosh, D J Wilkin
American Journal of Medical Genetics|March 10, 2000
Jeune asphyxiating thoracic dystrophy and short-rib polydactyly type III (Verma-Naumoff) are variants of the same disorderN C Ho, C A Francomano, M van Allen
American Journal of Medical Genetics|May 3, 1996
Progress in medical genetics: map-based gene discovery and the molecular pathology of skeletal dysplasiasV A McKusick, J S Amberger, C A Francomano
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1992
Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndromeW F Schwindinger, C A Francomano, M A Levine
Basic Life Sciences|January 1, 1988
Molecular genetic studies in achondroplasiaC A Francomano, P L Le, R E Pyeritz
Pediatric Dentistry|June 23, 1998
Pycnodysostosis: orofacial manifestations in two pediatric patientsA C O'Connell, M T Brennan, C A Francomano
The American Journal of Medicine|February 24, 2001
Minocycline-induced generalized postinflammatory elastolysisN C Ho, H Levy, C A Francomano, et al.
American Journal of Medical Genetics|August 5, 2000
Severe hypodontia and oral xanthomas in Alagille syndromeN C Ho, F Lacbawan, C A Francomano, et al.
Genomics|November 15, 1996
Brachydactyly type C gene maps to human chromsome 12q24M H Polymeropoulos, S E Ide, T Magyari, et al.
Human Molecular Genetics|June 19, 2001
Highly activated Fgfr3 with the K644M mutation causes prolonged survival in severe dwarf miceT Iwata, C L Li, C X Deng, et al.
Pageof 11

Showing results (11-20 of 101) with videos related to

Sort By:
Pageof 11
Current Opinion in Genetics & Development|June 1, 1996
Bone dysplasias in man: molecular insightsC A Francomano, I McIntosh, D J Wilkin
American Journal of Medical Genetics|March 10, 2000
Jeune asphyxiating thoracic dystrophy and short-rib polydactyly type III (Verma-Naumoff) are variants of the same disorderN C Ho, C A Francomano, M van Allen
American Journal of Medical Genetics|May 3, 1996
Progress in medical genetics: map-based gene discovery and the molecular pathology of skeletal dysplasiasV A McKusick, J S Amberger, C A Francomano
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1992
Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndromeW F Schwindinger, C A Francomano, M A Levine
Basic Life Sciences|January 1, 1988
Molecular genetic studies in achondroplasiaC A Francomano, P L Le, R E Pyeritz
Pediatric Dentistry|June 23, 1998
Pycnodysostosis: orofacial manifestations in two pediatric patientsA C O'Connell, M T Brennan, C A Francomano
The American Journal of Medicine|February 24, 2001
Minocycline-induced generalized postinflammatory elastolysisN C Ho, H Levy, C A Francomano, et al.
American Journal of Medical Genetics|August 5, 2000
Severe hypodontia and oral xanthomas in Alagille syndromeN C Ho, F Lacbawan, C A Francomano, et al.
Genomics|November 15, 1996
Brachydactyly type C gene maps to human chromsome 12q24M H Polymeropoulos, S E Ide, T Magyari, et al.
Human Molecular Genetics|June 19, 2001
Highly activated Fgfr3 with the K644M mutation causes prolonged survival in severe dwarf miceT Iwata, C L Li, C X Deng, et al.
Pageof 11