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 (81-90 of 146) with videos related to

Pageof 15
Sort By:
Nucleic Acids Research|December 11, 1991
Dinucleotide repeat polymorphism at D16S287H A Phillips, V J Hyland, K Holman, et al.
American Journal of Medical Genetics|July 12, 1996
Refinement of the background genetic map of Xq26-q27 and gene localisation for Börjeson-Forssman-Lehmann SyndromeA K Gedeon, H M Kozman, H Robinson, et al.
Annals of Neurology|August 12, 2000
A de novo mutation in sporadic nocturnal frontal lobe epilepsyH A Phillips, C Marini, I E Scheffer, et al.
Human Genetics|May 1, 1989
A linkage group with FRA16B (the fragile site at 16q22.1)J C Mulley, V J Hyland, A Fratini, et al.
Clinical Genetics|June 1, 1993
Direct molecular diagnosis of myotonic dystrophyB K Hecht, A Donnelly, A K Gedeon, et al.
Nature Genetics|May 1, 1995
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2H A Phillips, I E Scheffer, S F Berkovic, et al.
Lancet (London, England)|April 3, 1998
Deafness due to Pro250Arg mutation of FGFR3G E Hollway, G K Suthers, K M Battese, et al.
American Journal of Medical Genetics|June 1, 1994
Jackson-Weiss syndrome: clinical and radiological findings in a large kindred and exclusion of the gene from 7p21 and 5qterL C Adès, J C Mulley, I P Senga, et al.
American Journal of Medical Genetics|July 15, 1994
Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22A J Donnelly, K H Choo, H M Kozman, et al.
American Journal of Human Genetics|June 1, 1991
Fragile X syndrome: diagnosis using highly polymorphic microsatellite markersR I Richards, Y Shen, K Holman, et al.
Pageof 15

Showing results (81-90 of 146) with videos related to

Sort By:
Pageof 15
Nucleic Acids Research|December 11, 1991
Dinucleotide repeat polymorphism at D16S287H A Phillips, V J Hyland, K Holman, et al.
American Journal of Medical Genetics|July 12, 1996
Refinement of the background genetic map of Xq26-q27 and gene localisation for Börjeson-Forssman-Lehmann SyndromeA K Gedeon, H M Kozman, H Robinson, et al.
Annals of Neurology|August 12, 2000
A de novo mutation in sporadic nocturnal frontal lobe epilepsyH A Phillips, C Marini, I E Scheffer, et al.
Human Genetics|May 1, 1989
A linkage group with FRA16B (the fragile site at 16q22.1)J C Mulley, V J Hyland, A Fratini, et al.
Clinical Genetics|June 1, 1993
Direct molecular diagnosis of myotonic dystrophyB K Hecht, A Donnelly, A K Gedeon, et al.
Nature Genetics|May 1, 1995
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2H A Phillips, I E Scheffer, S F Berkovic, et al.
Lancet (London, England)|April 3, 1998
Deafness due to Pro250Arg mutation of FGFR3G E Hollway, G K Suthers, K M Battese, et al.
American Journal of Medical Genetics|June 1, 1994
Jackson-Weiss syndrome: clinical and radiological findings in a large kindred and exclusion of the gene from 7p21 and 5qterL C Adès, J C Mulley, I P Senga, et al.
American Journal of Medical Genetics|July 15, 1994
Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22A J Donnelly, K H Choo, H M Kozman, et al.
American Journal of Human Genetics|June 1, 1991
Fragile X syndrome: diagnosis using highly polymorphic microsatellite markersR I Richards, Y Shen, K Holman, et al.
Pageof 15