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 (51-60 of 102) with videos related to

Pageof 11
Sort By:
Journal of Medical Genetics|July 1, 1987
Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4C McKeown, A P Read, A Dodge, et al.
Journal of Medical Genetics|December 1, 1986
A register based system for gene tracking in Duchenne muscular dystrophyA P Read, L Kerzin-Storrar, R C Mountford, et al.
American Journal of Human Genetics|July 1, 1991
The gene for Treacher Collins syndrome maps to the long arm of chromosome 5M J Dixon, A P Read, D Donnai, et al.
Zeitschrift Fur Kinderchirurgie : Organ Der Deutschen, Der Schweizerischen Und Der Osterreichischen Gesellschaft Fur Kinderchirurgie = Surgery in Infancy and Childhood|December 1, 1988
A survey of neural tube defect pregnancies in north-west EnglandS H Bernard, J P Walsworth-Bell, M Super, et al.
Genomics|June 15, 1999
A complete physical contig and partial transcript map of the Williams syndrome critical regionE L Hockenhull, M J Carette, K Metcalfe, et al.
Human Molecular Genetics|July 1, 1997
Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosisM Tassabehji, K Metcalfe, D Donnai, et al.
Lancet (London, England)|October 3, 1987
Clinic experience of prenatal diagnosis of cystic fibrosis by use of linked DNA probesM Super, A Ivinson, M Schwarz, et al.
Advances in Oto-Rhino-Laryngology|January 25, 2007
The genetics of otosclerosis: pedigree studies and linkage analysisS R Saeed, M Briggs, C Lobo, et al.
Nature|February 13, 1992
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box geneM Tassabehji, A P Read, V E Newton, et al.
Nature Genetics|January 1, 1993
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2M Tassabehji, A P Read, V E Newton, et al.
Pageof 11

Showing results (51-60 of 102) with videos related to

Sort By:
Pageof 11
Journal of Medical Genetics|July 1, 1987
Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4C McKeown, A P Read, A Dodge, et al.
Journal of Medical Genetics|December 1, 1986
A register based system for gene tracking in Duchenne muscular dystrophyA P Read, L Kerzin-Storrar, R C Mountford, et al.
American Journal of Human Genetics|July 1, 1991
The gene for Treacher Collins syndrome maps to the long arm of chromosome 5M J Dixon, A P Read, D Donnai, et al.
Zeitschrift Fur Kinderchirurgie : Organ Der Deutschen, Der Schweizerischen Und Der Osterreichischen Gesellschaft Fur Kinderchirurgie = Surgery in Infancy and Childhood|December 1, 1988
A survey of neural tube defect pregnancies in north-west EnglandS H Bernard, J P Walsworth-Bell, M Super, et al.
Genomics|June 15, 1999
A complete physical contig and partial transcript map of the Williams syndrome critical regionE L Hockenhull, M J Carette, K Metcalfe, et al.
Human Molecular Genetics|July 1, 1997
Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosisM Tassabehji, K Metcalfe, D Donnai, et al.
Lancet (London, England)|October 3, 1987
Clinic experience of prenatal diagnosis of cystic fibrosis by use of linked DNA probesM Super, A Ivinson, M Schwarz, et al.
Advances in Oto-Rhino-Laryngology|January 25, 2007
The genetics of otosclerosis: pedigree studies and linkage analysisS R Saeed, M Briggs, C Lobo, et al.
Nature|February 13, 1992
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box geneM Tassabehji, A P Read, V E Newton, et al.
Nature Genetics|January 1, 1993
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2M Tassabehji, A P Read, V E Newton, et al.
Pageof 11