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 (41-50 of 101) with videos related to

Pageof 11
Sort By:
The Journal of Pediatrics|May 15, 1998
Sleep-disordered breathing in children with achondroplasiaP J Mogayzel, J L Carroll, G M Loughlin, et al.
Science (New York, N.Y.)|January 29, 1993
The skipping of constitutive exons in vivo induced by nonsense mutationsH C Dietz, D Valle, C A Francomano, et al.
Genomics|October 1, 1988
Macrorestriction mapping of COL4A1 and COL4A2 collagen genes on human chromosome 13q34G R Cutting, H H Kazazian, S E Antonarakis, et al.
American Journal of Human Genetics|November 1, 1994
High-resolution linkage-disequilibrium mapping of the cartilage-hair hypoplasia geneT Sulisalo, J Klockars, O Mäkitie, et al.
Genome Research|November 1, 1996
A nonsense mutation in the cathepsin K gene observed in a family with pycnodysostosisM R Johnson, M H Polymeropoulos, H L Vos, et al.
Cornea|July 1, 1992
Molecular genetic analysis in autosomal dominant keratoconusY S Rabinowitz, I H Maumenee, M K Lundergan, et al.
The Johns Hopkins Medical Journal|October 1, 1980
Pseudoxanthoma elasticum: treatment of gastrointestinal hemorrhage by arterial embolization and observations on autosomal dominant inheritanceJ R Cunningham, S M Lippman, W A Renie, et al.
Nature Genetics|June 1, 1995
The gene for pycnodysostosis maps to human chromosome 1cen-q21M H Polymeropoulos, R I Ortiz De Luna, S E Ide, et al.
American Journal of Medical Genetics|July 3, 1995
Confirmatory linkage of hypochondroplasia to chromosome arm 4pJ T Hecht, C A Herrera, G A Greenhaw, et al.
Nature Genetics|October 1, 1996
Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromesG A Bellus, K Gaudenz, E H Zackai, et al.
Pageof 11

Showing results (41-50 of 101) with videos related to

Sort By:
Pageof 11
The Journal of Pediatrics|May 15, 1998
Sleep-disordered breathing in children with achondroplasiaP J Mogayzel, J L Carroll, G M Loughlin, et al.
Science (New York, N.Y.)|January 29, 1993
The skipping of constitutive exons in vivo induced by nonsense mutationsH C Dietz, D Valle, C A Francomano, et al.
Genomics|October 1, 1988
Macrorestriction mapping of COL4A1 and COL4A2 collagen genes on human chromosome 13q34G R Cutting, H H Kazazian, S E Antonarakis, et al.
American Journal of Human Genetics|November 1, 1994
High-resolution linkage-disequilibrium mapping of the cartilage-hair hypoplasia geneT Sulisalo, J Klockars, O Mäkitie, et al.
Genome Research|November 1, 1996
A nonsense mutation in the cathepsin K gene observed in a family with pycnodysostosisM R Johnson, M H Polymeropoulos, H L Vos, et al.
Cornea|July 1, 1992
Molecular genetic analysis in autosomal dominant keratoconusY S Rabinowitz, I H Maumenee, M K Lundergan, et al.
The Johns Hopkins Medical Journal|October 1, 1980
Pseudoxanthoma elasticum: treatment of gastrointestinal hemorrhage by arterial embolization and observations on autosomal dominant inheritanceJ R Cunningham, S M Lippman, W A Renie, et al.
Nature Genetics|June 1, 1995
The gene for pycnodysostosis maps to human chromosome 1cen-q21M H Polymeropoulos, R I Ortiz De Luna, S E Ide, et al.
American Journal of Medical Genetics|July 3, 1995
Confirmatory linkage of hypochondroplasia to chromosome arm 4pJ T Hecht, C A Herrera, G A Greenhaw, et al.
Nature Genetics|October 1, 1996
Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromesG A Bellus, K Gaudenz, E H Zackai, et al.
Pageof 11