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P S Harper

Showing results (121-130 of 345) with videos related to

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Journal of Medical Genetics|January 1, 1992
Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales familiesJ C MacMillan, M Upadhyaya, P S Harper
The British Journal of Radiology|September 1, 1973
Morquio-Brailsford disease. A report of four affected sisters with absence of excessive keratan sulphate in the urineP Jenkins, G R Davies, P S Harper
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|June 15, 1988
Huntington's disease: prediction and preventionP S Harper, O W Quarrell, S Youngman
Clinical Genetics|January 23, 1999
Predictive testing for Huntington's disease: II. Qualitative findings from a study of uptake in South WalesJ Binedell, J R Soldan, P S Harper
PCR Methods and Applications|April 1, 1995
Amplification of the total coding sequence of the NF1 gene from peripheral blood lymphocyte RNAM H Shen, P S Harper, M Upadhyaya
Journal of Clinical Pathology|October 1, 1985
Recombinant DNA studies on stored necropsy brain samples from patients with Huntington's choreaM Upadhyaya, G P Reynolds, P S Harper
The British Journal of Radiology|September 1, 1973
Spondylo-epiphyseal dysplasia tarda: a report of four cases in two familiesP S Harper, P Jenkins, K M Laurence
The British Journal of Dermatology|March 1, 1980
Syndrome of ichthyosis, hepatosplenomegaly and cerebellar degeneration--steroid sulphatase activityP J Dykes, R Marks, P S Harper
Lancet (London, England)|July 9, 1983
Cloned gene probes for carrier detection in muscular dystrophyK E Davies, P S Harper, R Williamson
Human Molecular Genetics|November 1, 1993
Neurofibromatosis type 1 (NF1): the search for mutations by PCR-heteroduplex analysis on Hydrolink gelsM H Shen, P S Harper, M Upadhyaya
Pageof 35

Showing results (121-130 of 345) with videos related to

Sort By:
Pageof 35
Journal of Medical Genetics|January 1, 1992
Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales familiesJ C MacMillan, M Upadhyaya, P S Harper
The British Journal of Radiology|September 1, 1973
Morquio-Brailsford disease. A report of four affected sisters with absence of excessive keratan sulphate in the urineP Jenkins, G R Davies, P S Harper
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|June 15, 1988
Huntington's disease: prediction and preventionP S Harper, O W Quarrell, S Youngman
Clinical Genetics|January 23, 1999
Predictive testing for Huntington's disease: II. Qualitative findings from a study of uptake in South WalesJ Binedell, J R Soldan, P S Harper
PCR Methods and Applications|April 1, 1995
Amplification of the total coding sequence of the NF1 gene from peripheral blood lymphocyte RNAM H Shen, P S Harper, M Upadhyaya
Journal of Clinical Pathology|October 1, 1985
Recombinant DNA studies on stored necropsy brain samples from patients with Huntington's choreaM Upadhyaya, G P Reynolds, P S Harper
The British Journal of Radiology|September 1, 1973
Spondylo-epiphyseal dysplasia tarda: a report of four cases in two familiesP S Harper, P Jenkins, K M Laurence
The British Journal of Dermatology|March 1, 1980
Syndrome of ichthyosis, hepatosplenomegaly and cerebellar degeneration--steroid sulphatase activityP J Dykes, R Marks, P S Harper
Lancet (London, England)|July 9, 1983
Cloned gene probes for carrier detection in muscular dystrophyK E Davies, P S Harper, R Williamson
Human Molecular Genetics|November 1, 1993
Neurofibromatosis type 1 (NF1): the search for mutations by PCR-heteroduplex analysis on Hydrolink gelsM H Shen, P S Harper, M Upadhyaya
Pageof 35