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S M Huson

Showing results (51-60 of 85) with videos related to

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American Journal of Medical Genetics. Part A|January 19, 2010
Birth incidence and prevalence of tumor-prone syndromes: estimates from a UK family genetic register serviceD G Evans, E Howard, C Giblin, et al.
Brain : a Journal of Neurology|December 1, 1986
Cerebellar haemangioblastoma and von Hippel-Lindau diseaseS M Huson, P S Harper, M D Hourihan, et al.
Lancet (London, England)|July 6, 1991
Limb abnormalities and chorion villus samplingH V Firth, P A Boyd, P Chamberlain, et al.
Journal of Medical Genetics|September 1, 1995
Characterisation of germline mutations in the neurofibromatosis type 1 (NF1) geneM Upadhyaya, J Maynard, M Osborn, et al.
Journal of Medical Genetics|February 1, 1986
Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophyS M Huson, A L Meredith, M Sarfarazi, et al.
Journal of Medical Genetics|March 21, 2007
Women with neurofibromatosis 1 are at a moderately increased risk of developing breast cancer and should be considered for early screeningS Sharif, A Moran, S M Huson, et al.
Lancet (London, England)|March 30, 1991
Severe limb abnormalities after chorion villus sampling at 56-66 days' gestationH V Firth, P A Boyd, P Chamberlain, et al.
Genomics|February 1, 1989
Absence of linkage of hereditary motor and sensory neuropathy type I to chromosome 1 markersH R Middleton-Price, A E Harding, J Berciano, et al.
Journal of Medical Genetics|December 1, 1992
A genetic study of type 2 neurofibromatosis in the United Kingdom. II. Guidelines for genetic counsellingD G Evans, S M Huson, D Donnai, et al.
Human Genetics|January 1, 1985
The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locusD J Shaw, A L Meredith, M Sarfarazi, et al.
Pageof 9

Showing results (51-60 of 85) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics. Part A|January 19, 2010
Birth incidence and prevalence of tumor-prone syndromes: estimates from a UK family genetic register serviceD G Evans, E Howard, C Giblin, et al.
Brain : a Journal of Neurology|December 1, 1986
Cerebellar haemangioblastoma and von Hippel-Lindau diseaseS M Huson, P S Harper, M D Hourihan, et al.
Lancet (London, England)|July 6, 1991
Limb abnormalities and chorion villus samplingH V Firth, P A Boyd, P Chamberlain, et al.
Journal of Medical Genetics|September 1, 1995
Characterisation of germline mutations in the neurofibromatosis type 1 (NF1) geneM Upadhyaya, J Maynard, M Osborn, et al.
Journal of Medical Genetics|February 1, 1986
Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophyS M Huson, A L Meredith, M Sarfarazi, et al.
Journal of Medical Genetics|March 21, 2007
Women with neurofibromatosis 1 are at a moderately increased risk of developing breast cancer and should be considered for early screeningS Sharif, A Moran, S M Huson, et al.
Lancet (London, England)|March 30, 1991
Severe limb abnormalities after chorion villus sampling at 56-66 days' gestationH V Firth, P A Boyd, P Chamberlain, et al.
Genomics|February 1, 1989
Absence of linkage of hereditary motor and sensory neuropathy type I to chromosome 1 markersH R Middleton-Price, A E Harding, J Berciano, et al.
Journal of Medical Genetics|December 1, 1992
A genetic study of type 2 neurofibromatosis in the United Kingdom. II. Guidelines for genetic counsellingD G Evans, S M Huson, D Donnai, et al.
Human Genetics|January 1, 1985
The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locusD J Shaw, A L Meredith, M Sarfarazi, et al.
Pageof 9