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P W Lunt

Showing results (21-30 of 44) with videos related to

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Lancet (London, England)|November 24, 1990
DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral diseaseM Upadhyaya, P W Lunt, M Sarfarazi, et al.
Experimental and Clinical Endocrinology|May 1, 1991
Autosomal dominant inheritance of the tendency of develop thyroid autoantibodiesD I Phillips, L Prentice, S M McLachlan, et al.
Journal of Medical Genetics|October 1, 1991
A closely linked DNA marker for facioscapulohumeral disease on chromosome 4qM Upadhyaya, P W Lunt, M Sarfarazi, et al.
Journal of Medical Genetics|October 1, 1995
Duplication 2 (q11.2-q21): a previously unreported abnormalityL B Cooke, H Richards, P W Lunt, et al.
Annals of the New York Academy of Sciences|December 10, 1999
HMSN and HNPP. Laboratory service provision in the south west of England--two years' experienceM M Williams, L A Tyfield, P Jardine, et al.
Journal of Medical Genetics|June 1, 1997
Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHDM Upadhyaya, J Maynard, M T Rogers, et al.
Annals of the New York Academy of Sciences|November 1, 2017
HMSN and HNPP: Laboratory Service Provision in the South West of England-Two Years' ExperienceM M Williams, L A Tyfield, P Jardine, et al.
Lancet (London, England)|January 7, 1989
DNA probes in differential diagnosis of Becker muscular dystrophy and spinal muscular atrophyP W Lunt, W J Cumming, H Kingston, et al.
Clinical Dysmorphology|January 7, 2003
Siblings with Bohring-Opitz syndromeK L Greenhalgh, R A Newbury-Ecob, P W Lunt, et al.
The Journal of Pediatrics|September 15, 1999
Genetic analysis of the G4.5 gene in families with suspected Barth syndromeA M Cantlay, K Shokrollahi, J T Allen, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Lancet (London, England)|November 24, 1990
DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral diseaseM Upadhyaya, P W Lunt, M Sarfarazi, et al.
Experimental and Clinical Endocrinology|May 1, 1991
Autosomal dominant inheritance of the tendency of develop thyroid autoantibodiesD I Phillips, L Prentice, S M McLachlan, et al.
Journal of Medical Genetics|October 1, 1991
A closely linked DNA marker for facioscapulohumeral disease on chromosome 4qM Upadhyaya, P W Lunt, M Sarfarazi, et al.
Journal of Medical Genetics|October 1, 1995
Duplication 2 (q11.2-q21): a previously unreported abnormalityL B Cooke, H Richards, P W Lunt, et al.
Annals of the New York Academy of Sciences|December 10, 1999
HMSN and HNPP. Laboratory service provision in the south west of England--two years' experienceM M Williams, L A Tyfield, P Jardine, et al.
Journal of Medical Genetics|June 1, 1997
Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHDM Upadhyaya, J Maynard, M T Rogers, et al.
Annals of the New York Academy of Sciences|November 1, 2017
HMSN and HNPP: Laboratory Service Provision in the South West of England-Two Years' ExperienceM M Williams, L A Tyfield, P Jardine, et al.
Lancet (London, England)|January 7, 1989
DNA probes in differential diagnosis of Becker muscular dystrophy and spinal muscular atrophyP W Lunt, W J Cumming, H Kingston, et al.
Clinical Dysmorphology|January 7, 2003
Siblings with Bohring-Opitz syndromeK L Greenhalgh, R A Newbury-Ecob, P W Lunt, et al.
The Journal of Pediatrics|September 15, 1999
Genetic analysis of the G4.5 gene in families with suspected Barth syndromeA M Cantlay, K Shokrollahi, J T Allen, et al.
Pageof 5