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 C Mulley

Showing results (61-70 of 146) with videos related to

Pageof 15
Sort By:
American Journal of Medical Genetics|November 1, 1984
Genetic linkage analysis of epidermolysis bullosa simplex, Köbner typeJ C Mulley, C M Nicholls, D N Propert, et al.
American Journal of Medical Genetics|May 1, 1988
Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2)G R Sutherland, A K Gedeon, E A Haan, et al.
Nucleic Acids Research|December 25, 1991
Dinucleotide repeat polymorphisms at the D16S164, D16S168 and D16S186 loci at 16q21-q22.1H A Phillips, P Harris, R I Richards, et al.
Human Molecular Genetics|April 1, 1995
Localization of craniosynostosis Adelaide type to 4p16G E Hollway, H A Phillips, L C Adès, et al.
Journal of Medical Genetics|May 1, 1995
X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndromeA K Gedeon, M J Wilson, A C Colley, et al.
American Journal of Medical Genetics|May 1, 1988
X-linked mental retardation with dystonic movements of the handsM W Partington, J C Mulley, G R Sutherland, et al.
Human Genetics|December 1, 1990
Assignment of the gene for central core disease to chromosome 19E A Haan, C J Freemantle, J A McCure, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Integration of the cytogenetic and genetic linkage maps of human chromosome 16 using 50 physical intervals and 50 polymorphic lociH M Kozman, H A Phillips, D F Callen, et al.
American Journal of Medical Genetics|June 1, 1987
Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14J C Mulley, A K Gedeon, K A Thorn, et al.
Journal of Medical Genetics|December 1, 1987
Mapping the human alpha globin gene complex to 16p13.2----pterR N Simmers, J C Mulley, V J Hyland, et al.
Pageof 15

Showing results (61-70 of 146) with videos related to

Sort By:
Pageof 15
American Journal of Medical Genetics|November 1, 1984
Genetic linkage analysis of epidermolysis bullosa simplex, Köbner typeJ C Mulley, C M Nicholls, D N Propert, et al.
American Journal of Medical Genetics|May 1, 1988
Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2)G R Sutherland, A K Gedeon, E A Haan, et al.
Nucleic Acids Research|December 25, 1991
Dinucleotide repeat polymorphisms at the D16S164, D16S168 and D16S186 loci at 16q21-q22.1H A Phillips, P Harris, R I Richards, et al.
Human Molecular Genetics|April 1, 1995
Localization of craniosynostosis Adelaide type to 4p16G E Hollway, H A Phillips, L C Adès, et al.
Journal of Medical Genetics|May 1, 1995
X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndromeA K Gedeon, M J Wilson, A C Colley, et al.
American Journal of Medical Genetics|May 1, 1988
X-linked mental retardation with dystonic movements of the handsM W Partington, J C Mulley, G R Sutherland, et al.
Human Genetics|December 1, 1990
Assignment of the gene for central core disease to chromosome 19E A Haan, C J Freemantle, J A McCure, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Integration of the cytogenetic and genetic linkage maps of human chromosome 16 using 50 physical intervals and 50 polymorphic lociH M Kozman, H A Phillips, D F Callen, et al.
American Journal of Medical Genetics|June 1, 1987
Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14J C Mulley, A K Gedeon, K A Thorn, et al.
Journal of Medical Genetics|December 1, 1987
Mapping the human alpha globin gene complex to 16p13.2----pterR N Simmers, J C Mulley, V J Hyland, et al.
Pageof 15