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A L Meredith

Showing results (41-50 of 48) with videos related to

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British Medical Journal (Clinical Research Ed.)|November 22, 1986
Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophyA L Meredith, S M Huson, P W Lunt, et al.
Human Genetics|November 1, 1986
Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19D J Shaw, A L Meredith, J D Brook, et al.
Journal of Medical Genetics|December 1, 1992
Severity of chest disease in cystic fibrosis patients in relation to their genotypesL N al-Jader, A L Meredith, H C Ryley, et al.
Circulation Research|July 1, 1994
Alterations in cardiac gene expression during the transition from stable hypertrophy to heart failure. Marked upregulation of genes encoding extracellular matrix componentsM O Boluyt, L O'Neill, A L Meredith, et al.
Human Mutation|January 1, 1995
Cystic fibrosis mutation analysis: report from 22 U.K. regional genetics laboratoriesM J Schwarz, G M Malone, A Haworth, et al.
The Veterinary Record|January 26, 2011
Retrospective detection by negative contrast electron microscopy of faecal viral particles in free-living wild red squirrels (Sciurus vulgaris) with suspected enteropathy in Great BritainD J Everest, M F Stidworthy, E M Milne, et al.
Human Genetics|November 1, 1986
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19D J Shaw, A L Meredith, M Sarfarazi, et al.
The Veterinary Record|May 20, 1998
Staffing at veterinary schoolsS M Rhind, C L Scudamore, R E Clutton, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
British Medical Journal (Clinical Research Ed.)|November 22, 1986
Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophyA L Meredith, S M Huson, P W Lunt, et al.
Human Genetics|November 1, 1986
Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19D J Shaw, A L Meredith, J D Brook, et al.
Journal of Medical Genetics|December 1, 1992
Severity of chest disease in cystic fibrosis patients in relation to their genotypesL N al-Jader, A L Meredith, H C Ryley, et al.
Circulation Research|July 1, 1994
Alterations in cardiac gene expression during the transition from stable hypertrophy to heart failure. Marked upregulation of genes encoding extracellular matrix componentsM O Boluyt, L O'Neill, A L Meredith, et al.
Human Mutation|January 1, 1995
Cystic fibrosis mutation analysis: report from 22 U.K. regional genetics laboratoriesM J Schwarz, G M Malone, A Haworth, et al.
The Veterinary Record|January 26, 2011
Retrospective detection by negative contrast electron microscopy of faecal viral particles in free-living wild red squirrels (Sciurus vulgaris) with suspected enteropathy in Great BritainD J Everest, M F Stidworthy, E M Milne, et al.
Human Genetics|November 1, 1986
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19D J Shaw, A L Meredith, M Sarfarazi, et al.
The Veterinary Record|May 20, 1998
Staffing at veterinary schoolsS M Rhind, C L Scudamore, R E Clutton, et al.
Pageof 5