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

D Bourn
T Strachan

Human molecular genetics

Showing results (1-10 of 10) with videos related to

Pageof 1
Sort By:
Human Molecular Genetics|May 1, 1994
Germline mutations in the neurofibromatosis type 2 tumour suppressor geneD Bourn, S A Carter, S Mason, et al.
Human Molecular Genetics|February 5, 1999
H4 acetylation, XIST RNA and replication timing are coincident and define x;autosome boundaries in two abnormal X chromosomesA M Keohane, A L Barlow, J Waters, et al.
Human Molecular Genetics|June 1, 1993
A disease-associated germline deletion maps the type 2 neurofibromatosis (NF2) gene between the Ewing sarcoma region and the leukaemia inhibitory factor locusC J Watson, L Gaunt, G Evans, et al.
Human Molecular Genetics|May 23, 1998
A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrainM Lako, S Lindsay, P Bullen, et al.
Human Molecular Genetics|March 1, 1994
A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2pR Bashir, T Strachan, S Keers, 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.
Human Molecular Genetics|December 23, 1999
Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genesF Fougerousse, P Bullen, M Herasse, et al.
Human Molecular Genetics|April 6, 2000
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndromeM Clement-Jones, S Schiller, E Rao, et al.
Human Molecular Genetics|April 18, 2000
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pumpR Sudbrak, J Brown, C Dobson-Stone, et al.
Human Molecular Genetics|August 11, 1999
ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation classV L Ruiz-Perez, S A Carter, E Healy, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Human Molecular Genetics|May 1, 1994
Germline mutations in the neurofibromatosis type 2 tumour suppressor geneD Bourn, S A Carter, S Mason, et al.
Human Molecular Genetics|February 5, 1999
H4 acetylation, XIST RNA and replication timing are coincident and define x;autosome boundaries in two abnormal X chromosomesA M Keohane, A L Barlow, J Waters, et al.
Human Molecular Genetics|June 1, 1993
A disease-associated germline deletion maps the type 2 neurofibromatosis (NF2) gene between the Ewing sarcoma region and the leukaemia inhibitory factor locusC J Watson, L Gaunt, G Evans, et al.
Human Molecular Genetics|May 23, 1998
A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrainM Lako, S Lindsay, P Bullen, et al.
Human Molecular Genetics|March 1, 1994
A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2pR Bashir, T Strachan, S Keers, 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.
Human Molecular Genetics|December 23, 1999
Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genesF Fougerousse, P Bullen, M Herasse, et al.
Human Molecular Genetics|April 6, 2000
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndromeM Clement-Jones, S Schiller, E Rao, et al.
Human Molecular Genetics|April 18, 2000
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pumpR Sudbrak, J Brown, C Dobson-Stone, et al.
Human Molecular Genetics|August 11, 1999
ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation classV L Ruiz-Perez, S A Carter, E Healy, et al.
Pageof 1