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D O Robinson

Showing results (21-30 of 49) with videos related to

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Leukemia|October 12, 1999
Identification of false-positive CBFbeta/MYH11 RT-PCR resultsS M Hackwell, D O Robinson, J F Harvey, et al.
Archives of Medical Research|April 18, 2000
Functional Xp disomy and hypomelanosis of ItoH Rivera, L S Correa-Cerro, D O Robinson, et al.
Human Genetics|January 1, 1995
Fluorescence in situ hybridisation studies provide evidence for somatic mosaicism in de novo dystrophin gene deletionsD J Bunyan, J A Crolla, A L Collins, et al.
Scandinavian Journal of Gastroenterology|January 1, 1977
Pancreatitis and renal diseaseD O Robinson, M H Alp, A K Grant, et al.
Journal of Medical Genetics|May 2, 2006
Oculopharyngeal muscular dystrophy: a point mutation which mimics the effect of the PABPN1 gene triplet repeat expansion mutationD O Robinson, A J Wills, S R Hammans, et al.
Clinical Genetics|January 23, 1999
Paternal uniparental disomy of chromosome 6 and transient neonatal diabetes mellitusR J Gardner, D O Robinson, L Lamont, et al.
Genetical Research|October 1, 1990
The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysisD O Robinson, Y Boyd, D Cockburn, et al.
Human Genetics|May 1, 1997
A small intraexonic deletion within the dystrophin gene suggests a possible mechanism of mutagenesisD O Robinson, D J Bunyan, H A Gabb, et al.
Diabetologia|August 18, 2001
Maturity onset diabetes of the young (MODY) and early onset Type II diabetes are not caused by loss of imprinting at the transient neonatal diabetes (TNDM) locusJ Shield, K Owen, D O Robinson, et al.
Journal of Medical Genetics|May 14, 2008
Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndromeH Bullman, M Lever, D O Robinson, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Leukemia|October 12, 1999
Identification of false-positive CBFbeta/MYH11 RT-PCR resultsS M Hackwell, D O Robinson, J F Harvey, et al.
Archives of Medical Research|April 18, 2000
Functional Xp disomy and hypomelanosis of ItoH Rivera, L S Correa-Cerro, D O Robinson, et al.
Human Genetics|January 1, 1995
Fluorescence in situ hybridisation studies provide evidence for somatic mosaicism in de novo dystrophin gene deletionsD J Bunyan, J A Crolla, A L Collins, et al.
Scandinavian Journal of Gastroenterology|January 1, 1977
Pancreatitis and renal diseaseD O Robinson, M H Alp, A K Grant, et al.
Journal of Medical Genetics|May 2, 2006
Oculopharyngeal muscular dystrophy: a point mutation which mimics the effect of the PABPN1 gene triplet repeat expansion mutationD O Robinson, A J Wills, S R Hammans, et al.
Clinical Genetics|January 23, 1999
Paternal uniparental disomy of chromosome 6 and transient neonatal diabetes mellitusR J Gardner, D O Robinson, L Lamont, et al.
Genetical Research|October 1, 1990
The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysisD O Robinson, Y Boyd, D Cockburn, et al.
Human Genetics|May 1, 1997
A small intraexonic deletion within the dystrophin gene suggests a possible mechanism of mutagenesisD O Robinson, D J Bunyan, H A Gabb, et al.
Diabetologia|August 18, 2001
Maturity onset diabetes of the young (MODY) and early onset Type II diabetes are not caused by loss of imprinting at the transient neonatal diabetes (TNDM) locusJ Shield, K Owen, D O Robinson, et al.
Journal of Medical Genetics|May 14, 2008
Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndromeH Bullman, M Lever, D O Robinson, et al.
Pageof 5