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

A P Read

Showing results (61-70 of 102) with videos related to

Pageof 11
Sort By:
Journal of Medical Genetics|July 1, 1989
Testing for cystic fibrosis using allelic associationA J Ivinson, A P Read, R Harris, et al.
Journal of Medical Genetics|January 1, 1988
Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosomeK E Davies, T J Smith, S Bundey, et al.
Human Genetics|October 1, 1988
Patterns of exon deletions in Duchenne and Becker muscular dystrophyA P Read, R C Mountford, S M Forrest, et al.
Transplantation|November 1, 1981
Matching for properdin factor B (Bf) in renal transplantationP A Dyer, P T Klouda, R W Johnson, et al.
Lancet (London, England)|January 7, 1989
DNA probes in differential diagnosis of Becker muscular dystrophy and spinal muscular atrophyP W Lunt, W J Cumming, H Kingston, et al.
International Journal of Pediatric Otorhinolaryngology|June 1, 1995
Gene linkage and genetic deafnessC W Cremers, S D Brown, K P Steel, et al.
Journal of Medical Genetics|February 5, 2003
Using case study comparisons to explore genotype-phenotype correlations in Williams-Beuren syndromeA Karmiloff-Smith, J Grant, S Ewing, et al.
Human Molecular Genetics|July 1, 1994
PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouseM Tassabehji, V E Newton, K Leverton, et al.
Journal of Medical Genetics|December 24, 1998
Differential diagnosis of type 2 neurofibromatosis: molecular discrimination of NF2 and sporadic vestibular schwannomasC L Wu, N Thakker, W Neary, et al.
Human Molecular Genetics|June 13, 1998
An elastin gene mutation producing abnormal tropoelastin and abnormal elastic fibres in a patient with autosomal dominant cutis laxaM Tassabehji, K Metcalfe, J Hurst, et al.
Pageof 11

Showing results (61-70 of 102) with videos related to

Sort By:
Pageof 11
Journal of Medical Genetics|July 1, 1989
Testing for cystic fibrosis using allelic associationA J Ivinson, A P Read, R Harris, et al.
Journal of Medical Genetics|January 1, 1988
Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosomeK E Davies, T J Smith, S Bundey, et al.
Human Genetics|October 1, 1988
Patterns of exon deletions in Duchenne and Becker muscular dystrophyA P Read, R C Mountford, S M Forrest, et al.
Transplantation|November 1, 1981
Matching for properdin factor B (Bf) in renal transplantationP A Dyer, P T Klouda, R W Johnson, et al.
Lancet (London, England)|January 7, 1989
DNA probes in differential diagnosis of Becker muscular dystrophy and spinal muscular atrophyP W Lunt, W J Cumming, H Kingston, et al.
International Journal of Pediatric Otorhinolaryngology|June 1, 1995
Gene linkage and genetic deafnessC W Cremers, S D Brown, K P Steel, et al.
Journal of Medical Genetics|February 5, 2003
Using case study comparisons to explore genotype-phenotype correlations in Williams-Beuren syndromeA Karmiloff-Smith, J Grant, S Ewing, et al.
Human Molecular Genetics|July 1, 1994
PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouseM Tassabehji, V E Newton, K Leverton, et al.
Journal of Medical Genetics|December 24, 1998
Differential diagnosis of type 2 neurofibromatosis: molecular discrimination of NF2 and sporadic vestibular schwannomasC L Wu, N Thakker, W Neary, et al.
Human Molecular Genetics|June 13, 1998
An elastin gene mutation producing abnormal tropoelastin and abnormal elastic fibres in a patient with autosomal dominant cutis laxaM Tassabehji, K Metcalfe, J Hurst, et al.
Pageof 11