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E M Rosser

Showing results (1-10 of 8) with videos related to

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Journal of Medical Genetics|December 1, 1996
Cancer families: what risks are they given and do the risks affect management?E M Rosser, J A Hurst, C J Chapman
Clinical Dysmorphology|July 1, 1996
Nance-Sweeney chondrodysplasia--a further case?E M Rosser, C M Hall, J Harper, et al.
Clinical Dysmorphology|April 1, 1996
Serpentine fibula syndrome: expansion of the phenotype with three affected siblingsE M Rosser, N P Mann, C M Hall, et al.
Clinical Dysmorphology|February 2, 2002
Lethal acrofacial dysostosis, pre- and post-axial defects of the hands, and bilateral renal agenesisA W Bates, C M Hall, H Morgan, et al.
American Journal of Medical Genetics|September 11, 1995
Geleophysic dysplasia: a report of three affected boys--prenatal ultrasound does not detect recurrenceE M Rosser, A R Wilkinson, J A Hurst, et al.
Clinical Dysmorphology|May 8, 1998
Three patients with the osteochondrodysplasia and hypertrichosis syndrome--Cantu syndromeE M Rosser, H Kaariainen, J A Hurst, et al.
Neurology|April 30, 2008
Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN)M A Kurian, N V Morgan, L MacPherson, et al.
Journal of Molecular Endocrinology|September 29, 2012
Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signallingD Hanson, P G Murray, T Coulson, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of Medical Genetics|December 1, 1996
Cancer families: what risks are they given and do the risks affect management?E M Rosser, J A Hurst, C J Chapman
Clinical Dysmorphology|July 1, 1996
Nance-Sweeney chondrodysplasia--a further case?E M Rosser, C M Hall, J Harper, et al.
Clinical Dysmorphology|April 1, 1996
Serpentine fibula syndrome: expansion of the phenotype with three affected siblingsE M Rosser, N P Mann, C M Hall, et al.
Clinical Dysmorphology|February 2, 2002
Lethal acrofacial dysostosis, pre- and post-axial defects of the hands, and bilateral renal agenesisA W Bates, C M Hall, H Morgan, et al.
American Journal of Medical Genetics|September 11, 1995
Geleophysic dysplasia: a report of three affected boys--prenatal ultrasound does not detect recurrenceE M Rosser, A R Wilkinson, J A Hurst, et al.
Clinical Dysmorphology|May 8, 1998
Three patients with the osteochondrodysplasia and hypertrichosis syndrome--Cantu syndromeE M Rosser, H Kaariainen, J A Hurst, et al.
Neurology|April 30, 2008
Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN)M A Kurian, N V Morgan, L MacPherson, et al.
Journal of Molecular Endocrinology|September 29, 2012
Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signallingD Hanson, P G Murray, T Coulson, et al.
Pageof 1