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S M Huson

Showing results (21-30 of 85) with videos related to

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American Journal of Medical Genetics|December 1, 1988
Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13L Brueton, S M Huson, R M Winter, et al.
Journal of Medical Genetics|September 1, 1987
Further exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markersM Upadhyaya, M Sarfarazi, S M Huson, et al.
Journal of Medical Genetics|November 14, 1997
The phenotypic effects of chromosome rearrangement involving bands 7q21.3 and 22q13.3A Slavotinek, E Maher, P Gregory, et al.
Annals of Neurology|May 13, 1999
A novel point mutation in X-linked adrenoleukodystrophy presenting as a spinocerebellar degenerationE Dunne, N M Hyman, S M Huson, et al.
The British Journal of Dermatology|March 17, 2001
Pigmentary anomalies in ataxia--telangiectasia: a clue to diagnosis and an example of twin spottingN P Khumalo, D V Joss, S M Huson, et al.
Clinical Genetics|July 19, 2002
Service provision of complex mutation analysis: a technical and economic appraisal using dystrophin point mutation analysis as an exampleJohn Nixon, D Cockburn, J Hopkin, et al.
Family Practice|May 13, 1999
Family history taking and genetic counselling in primary careP Rose, E Humm, K Hey, et al.
Journal of Medical Genetics|March 1, 1990
Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?L A Brueton, S M Huson, B Farren, et al.
Journal of Medical Genetics|November 1, 1989
A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severityS M Huson, D A Compston, P Clark, et al.
Journal of Medical Genetics|November 1, 1989
Partial monosomy 3q in a boy with short stature, developmental delay, and mild dysmorphic featuresL A Brueton, J C Barber, S M Huson, et al.
Pageof 9

Showing results (21-30 of 85) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics|December 1, 1988
Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13L Brueton, S M Huson, R M Winter, et al.
Journal of Medical Genetics|September 1, 1987
Further exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markersM Upadhyaya, M Sarfarazi, S M Huson, et al.
Journal of Medical Genetics|November 14, 1997
The phenotypic effects of chromosome rearrangement involving bands 7q21.3 and 22q13.3A Slavotinek, E Maher, P Gregory, et al.
Annals of Neurology|May 13, 1999
A novel point mutation in X-linked adrenoleukodystrophy presenting as a spinocerebellar degenerationE Dunne, N M Hyman, S M Huson, et al.
The British Journal of Dermatology|March 17, 2001
Pigmentary anomalies in ataxia--telangiectasia: a clue to diagnosis and an example of twin spottingN P Khumalo, D V Joss, S M Huson, et al.
Clinical Genetics|July 19, 2002
Service provision of complex mutation analysis: a technical and economic appraisal using dystrophin point mutation analysis as an exampleJohn Nixon, D Cockburn, J Hopkin, et al.
Family Practice|May 13, 1999
Family history taking and genetic counselling in primary careP Rose, E Humm, K Hey, et al.
Journal of Medical Genetics|March 1, 1990
Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?L A Brueton, S M Huson, B Farren, et al.
Journal of Medical Genetics|November 1, 1989
A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severityS M Huson, D A Compston, P Clark, et al.
Journal of Medical Genetics|November 1, 1989
Partial monosomy 3q in a boy with short stature, developmental delay, and mild dysmorphic featuresL A Brueton, J C Barber, S M Huson, et al.
Pageof 9