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

M A Aldred

Showing results (11-20 of 26) with videos related to

Pageof 3
Sort By:
Blood|October 1, 1996
Interstitial deletion constitutes the major mechanism for loss of heterozygosity on chromosome 20q in polycythemia veraF A Asimakopoulos, J G Gilbert, M A Aldred, et al.
Lancet (London, England)|September 3, 1988
Familial polyposis coliM A Aldred, M Rees, K Tsioupra, et al.
Clinical Genetics|May 1, 1993
Linkage analysis in a family with complete type congenital stationary night blindness with and without myopiaK L Dry, D B Van Dorp, M A Aldred, et al.
Journal of Medical Genetics|November 10, 2000
Germline mosaicism for a GNAS1 mutation and Albright hereditary osteodystrophyM A Aldred, R J Bagshaw, K Macdermot, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome XM A Aldred, T Flint, R Vossen, et al.
American Journal of Human Genetics|November 1, 1991
Risk calculation in retinitis pigmentosaS M Holloway, L Strain, A E Shrimpton, et al.
Journal of Medical Genetics|November 1, 1994
Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 lociM A Aldred, P W Teague, M Jay, et al.
Journal of Medical Genetics|July 1, 1991
Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindredA F Wright, S S Bhattacharya, M A Aldred, et al.
American Journal of Human Genetics|July 1, 1994
Heterogeneity analysis in 40 X-linked retinitis pigmentosa familiesP W Teague, M A Aldred, M Jay, et al.
Human Molecular Genetics|December 1, 1995
Identification of a novel gene, ETX1 from Xp21.1, a candidate gene for X-linked retintis pigmentosa (RP3)K L Dry, M A Aldred, A J Edgar, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Blood|October 1, 1996
Interstitial deletion constitutes the major mechanism for loss of heterozygosity on chromosome 20q in polycythemia veraF A Asimakopoulos, J G Gilbert, M A Aldred, et al.
Lancet (London, England)|September 3, 1988
Familial polyposis coliM A Aldred, M Rees, K Tsioupra, et al.
Clinical Genetics|May 1, 1993
Linkage analysis in a family with complete type congenital stationary night blindness with and without myopiaK L Dry, D B Van Dorp, M A Aldred, et al.
Journal of Medical Genetics|November 10, 2000
Germline mosaicism for a GNAS1 mutation and Albright hereditary osteodystrophyM A Aldred, R J Bagshaw, K Macdermot, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome XM A Aldred, T Flint, R Vossen, et al.
American Journal of Human Genetics|November 1, 1991
Risk calculation in retinitis pigmentosaS M Holloway, L Strain, A E Shrimpton, et al.
Journal of Medical Genetics|November 1, 1994
Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 lociM A Aldred, P W Teague, M Jay, et al.
Journal of Medical Genetics|July 1, 1991
Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindredA F Wright, S S Bhattacharya, M A Aldred, et al.
American Journal of Human Genetics|July 1, 1994
Heterogeneity analysis in 40 X-linked retinitis pigmentosa familiesP W Teague, M A Aldred, M Jay, et al.
Human Molecular Genetics|December 1, 1995
Identification of a novel gene, ETX1 from Xp21.1, a candidate gene for X-linked retintis pigmentosa (RP3)K L Dry, M A Aldred, A J Edgar, et al.
Pageof 3