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P Lunt

Showing results (11-20 of 24) with videos related to

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American Journal of Human Genetics|August 1, 1992
The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, P Lunt, M Sarfarazi, et al.
Human Mutation|January 1, 1994
Two new rhodopsin transversion mutations (L40R; M216K) in families with autosomal dominant retinitis pigmentosaM al-Maghtheh, C Inglehearn, P Lunt, et al.
Regional Anesthesia and Pain Medicine|December 10, 1999
Cerebrospinal fluid cytokine levels after surgery with spinal or general anesthesiaM P Yeager, P Lunt, J Arruda, et al.
Journal of Intellectual Disability Research : JIDR|October 1, 1994
The association between Coffin-Lowry syndrome and psychosis: a family studyU Sivagamasundari, H Fernando, P Jardine, et al.
Lancet (London, England)|April 15, 1995
Early morphological evidence of autosomal recessive polycystic kidney diseaseK Zerres, G Mücher, S Rudnik-Schöneborn, et al.
Journal of Medical Genetics|August 1, 1989
An exclusion map for facioscapulohumeral (Landouzy-Déjérine) diseaseM Sarfarazi, M Upadhyaya, G Padberg, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1991
Autosomal dominant inheritance of autoantibodies to thyroid peroxidase and thyroglobulin--studies in families not selected for autoimmune thyroid diseaseD Phillips, L Prentice, M Upadhyaya, et al.
American Journal of Human Genetics|August 1, 1992
Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortiumM Sarfarazi, C Wijmenga, M Upadhyaya, et al.
Journal of Medical Genetics|August 1, 1989
Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral diseaseT Siddique, H Roper, M A Pericak-Vance, et al.
Human Molecular Genetics|December 6, 2001
Mutations in the general transcription factor TFIIH result in beta-thalassaemia in individuals with trichothiodystrophyV Viprakasit, R J Gibbons, B C Broughton, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
American Journal of Human Genetics|August 1, 1992
The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, P Lunt, M Sarfarazi, et al.
Human Mutation|January 1, 1994
Two new rhodopsin transversion mutations (L40R; M216K) in families with autosomal dominant retinitis pigmentosaM al-Maghtheh, C Inglehearn, P Lunt, et al.
Regional Anesthesia and Pain Medicine|December 10, 1999
Cerebrospinal fluid cytokine levels after surgery with spinal or general anesthesiaM P Yeager, P Lunt, J Arruda, et al.
Journal of Intellectual Disability Research : JIDR|October 1, 1994
The association between Coffin-Lowry syndrome and psychosis: a family studyU Sivagamasundari, H Fernando, P Jardine, et al.
Lancet (London, England)|April 15, 1995
Early morphological evidence of autosomal recessive polycystic kidney diseaseK Zerres, G Mücher, S Rudnik-Schöneborn, et al.
Journal of Medical Genetics|August 1, 1989
An exclusion map for facioscapulohumeral (Landouzy-Déjérine) diseaseM Sarfarazi, M Upadhyaya, G Padberg, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1991
Autosomal dominant inheritance of autoantibodies to thyroid peroxidase and thyroglobulin--studies in families not selected for autoimmune thyroid diseaseD Phillips, L Prentice, M Upadhyaya, et al.
American Journal of Human Genetics|August 1, 1992
Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortiumM Sarfarazi, C Wijmenga, M Upadhyaya, et al.
Journal of Medical Genetics|August 1, 1989
Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral diseaseT Siddique, H Roper, M A Pericak-Vance, et al.
Human Molecular Genetics|December 6, 2001
Mutations in the general transcription factor TFIIH result in beta-thalassaemia in individuals with trichothiodystrophyV Viprakasit, R J Gibbons, B C Broughton, et al.
Pageof 3