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P J Hallam

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Annals of the Royal College of Surgeons of England|July 12, 2003
Analysis of the referral pattern to a supraregional bone and soft tissue tumour serviceN Ashwood, J D Witt, P J Hallam, et al.
Annals of Neurology|May 1, 1992
Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1)P J Hallam, A E Harding, J Berciano, et al.
Journal of Medical Genetics|July 1, 1995
Population differences in the frequency of the factor V Leiden variant among people with clinically symptomatic protein C deficiencyP J Hallam, D S Millar, M Krawczak, et al.
Clinical Genetics|October 27, 1998
Three novel PROC gene lesions causing protein C deficiencyP J Hallam, P Mannucci, A Tripodi, et al.
Blood|May 1, 1996
Severe perinatal thrombosis in double and triple heterozygous offspring of a family segregating two independent protein S mutations and a protein C mutationC J Formstone, P J Hallam, E G Tuddenham, et al.
Human Genetics|April 1, 1995
A novel missense mutation (Thr176-->Ile) at the putative hinge of the neo N-terminus of activated protein CP J Hallam, A I Wacey, P M Mannucci, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Annals of the Royal College of Surgeons of England|July 12, 2003
Analysis of the referral pattern to a supraregional bone and soft tissue tumour serviceN Ashwood, J D Witt, P J Hallam, et al.
Annals of Neurology|May 1, 1992
Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1)P J Hallam, A E Harding, J Berciano, et al.
Journal of Medical Genetics|July 1, 1995
Population differences in the frequency of the factor V Leiden variant among people with clinically symptomatic protein C deficiencyP J Hallam, D S Millar, M Krawczak, et al.
Clinical Genetics|October 27, 1998
Three novel PROC gene lesions causing protein C deficiencyP J Hallam, P Mannucci, A Tripodi, et al.
Blood|May 1, 1996
Severe perinatal thrombosis in double and triple heterozygous offspring of a family segregating two independent protein S mutations and a protein C mutationC J Formstone, P J Hallam, E G Tuddenham, et al.
Human Genetics|April 1, 1995
A novel missense mutation (Thr176-->Ile) at the putative hinge of the neo N-terminus of activated protein CP J Hallam, A I Wacey, P M Mannucci, et al.
Pageof 1