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R C Trembath

Showing results (11-20 of 86) with videos related to

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QJM : Monthly Journal of the Association of Physicians|August 12, 2008
Translational medicine and the NIHR Biomedical Research Centre conceptK Snape, R C Trembath, G M Lord
Verhandlungen Der Deutschen Gesellschaft Fur Innere Medizin|January 1, 1987
DNA polymorphisms of the insulin receptor gene and non-insulin-dependent diabetes mellitusR C Trembath, S Li, D J Galton
Lancet (London, England)|May 1, 1993
Chromosome 11q13 and atopy underlying atopic eczemaR Coleman, R C Trembath, J I Harper
Thorax|October 20, 2001
New insights into the pathogenesis and treatment of primary pulmonary hypertensionN Rudarakanchana, R C Trembath, N W Morrell
The Journal of Investigative Dermatology|February 1, 1995
Exclusion of interleukin-1 receptor antagonist as a primary disease determinant for psoriasisJ L Rosbotham, J N Barker, R C Trembath
Journal of Medical Genetics|October 1, 1996
Isolated autosomal dominant type E brachydactyly: exclusion of linkage to candidate regions 2q37 and 20q13M E Oude Luttikhuis, D K Williams, R C Trembath
Journal of Medical Genetics|June 27, 1998
The diagnosis of Liddle syndrome by identification of a mutation in the beta subunit of the epithelial sodium channelS N Jackson, B Williams, P Houtman, et al.
Genomics|May 15, 1994
Characterization of a de novo 43-bp deletion of the Gs alpha gene (GNAS1) in Albright hereditary osteodystrophyM E Luttikhuis, L C Wilson, J V Leonard, et al.
Ophthalmic Genetics|June 1, 1996
Familial exudative vitreoretinopathy linked to D11S533 in a large Asian family with consanguinityS M Price, N Periam, A Humphries, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|March 16, 2001
Immunolocalisation of BMPR-II and TGF-ß type I and II receptors in primary plexogenic pulmonary hypertensionC Atkinson, S Stewart, T Imamura, et al.
Pageof 9

Showing results (11-20 of 86) with videos related to

Sort By:
Pageof 9
QJM : Monthly Journal of the Association of Physicians|August 12, 2008
Translational medicine and the NIHR Biomedical Research Centre conceptK Snape, R C Trembath, G M Lord
Verhandlungen Der Deutschen Gesellschaft Fur Innere Medizin|January 1, 1987
DNA polymorphisms of the insulin receptor gene and non-insulin-dependent diabetes mellitusR C Trembath, S Li, D J Galton
Lancet (London, England)|May 1, 1993
Chromosome 11q13 and atopy underlying atopic eczemaR Coleman, R C Trembath, J I Harper
Thorax|October 20, 2001
New insights into the pathogenesis and treatment of primary pulmonary hypertensionN Rudarakanchana, R C Trembath, N W Morrell
The Journal of Investigative Dermatology|February 1, 1995
Exclusion of interleukin-1 receptor antagonist as a primary disease determinant for psoriasisJ L Rosbotham, J N Barker, R C Trembath
Journal of Medical Genetics|October 1, 1996
Isolated autosomal dominant type E brachydactyly: exclusion of linkage to candidate regions 2q37 and 20q13M E Oude Luttikhuis, D K Williams, R C Trembath
Journal of Medical Genetics|June 27, 1998
The diagnosis of Liddle syndrome by identification of a mutation in the beta subunit of the epithelial sodium channelS N Jackson, B Williams, P Houtman, et al.
Genomics|May 15, 1994
Characterization of a de novo 43-bp deletion of the Gs alpha gene (GNAS1) in Albright hereditary osteodystrophyM E Luttikhuis, L C Wilson, J V Leonard, et al.
Ophthalmic Genetics|June 1, 1996
Familial exudative vitreoretinopathy linked to D11S533 in a large Asian family with consanguinityS M Price, N Periam, A Humphries, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|March 16, 2001
Immunolocalisation of BMPR-II and TGF-ß type I and II receptors in primary plexogenic pulmonary hypertensionC Atkinson, S Stewart, T Imamura, et al.
Pageof 9