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A L Meredith

Showing results (31-40 of 48) with videos related to

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Journal of Medical Genetics|February 1, 1986
Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophyS M Huson, A L Meredith, M Sarfarazi, et al.
Journal of Medical Genetics|February 1, 1986
Gene mapping and chromosome 19D J Shaw, J D Brook, A L Meredith, et al.
Journal of Medical Genetics|November 1, 1992
Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophyJ Myring, A L Meredith, H G Harley, et al.
Annals of the New York Academy of Sciences|January 1, 1986
Evidence against linkage of von Recklinghausen neurofibromatosis and chromosome 19 markersS M Huson, A L Meredith, M Sarfarazi, et al.
Human Genetics|January 1, 1985
The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locusD J Shaw, A L Meredith, M Sarfarazi, et al.
Clinical Genetics|March 1, 1993
Huntington's disease: predictive testing and the molecular genetics laboratoryL P Lazarou, A L Meredith, J M Myring, et al.
The Veterinary Record|August 24, 2010
Epidemiological and postmortem findings in 262 red squirrels (Sciurus vulgaris) in Scotland, 2005 to 2009J P LaRose, A L Meredith, D J Everest, et al.
Journal of Medical Genetics|September 1, 1990
Genetic analysis of treated and untreated phenylketonuria in one familyL A Tyfield, A L Meredith, M J Osborn, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 2, 2007
Mosaicism in autosomal dominant polycystic kidney disease revealed by genetic testing to enable living related renal transplantationA Connor, P W Lunt, C Dolling, et al.
Neuroscience|January 17, 2016
MaxiK channel interactome reveals its interaction with GABA transporter 3 and heat shock protein 60 in the mammalian brainH Singh, M Li, L Hall, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Journal of Medical Genetics|February 1, 1986
Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophyS M Huson, A L Meredith, M Sarfarazi, et al.
Journal of Medical Genetics|February 1, 1986
Gene mapping and chromosome 19D J Shaw, J D Brook, A L Meredith, et al.
Journal of Medical Genetics|November 1, 1992
Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophyJ Myring, A L Meredith, H G Harley, et al.
Annals of the New York Academy of Sciences|January 1, 1986
Evidence against linkage of von Recklinghausen neurofibromatosis and chromosome 19 markersS M Huson, A L Meredith, M Sarfarazi, et al.
Human Genetics|January 1, 1985
The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locusD J Shaw, A L Meredith, M Sarfarazi, et al.
Clinical Genetics|March 1, 1993
Huntington's disease: predictive testing and the molecular genetics laboratoryL P Lazarou, A L Meredith, J M Myring, et al.
The Veterinary Record|August 24, 2010
Epidemiological and postmortem findings in 262 red squirrels (Sciurus vulgaris) in Scotland, 2005 to 2009J P LaRose, A L Meredith, D J Everest, et al.
Journal of Medical Genetics|September 1, 1990
Genetic analysis of treated and untreated phenylketonuria in one familyL A Tyfield, A L Meredith, M J Osborn, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 2, 2007
Mosaicism in autosomal dominant polycystic kidney disease revealed by genetic testing to enable living related renal transplantationA Connor, P W Lunt, C Dolling, et al.
Neuroscience|January 17, 2016
MaxiK channel interactome reveals its interaction with GABA transporter 3 and heat shock protein 60 in the mammalian brainH Singh, M Li, L Hall, et al.
Pageof 5