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R C Trembath

Showing results (71-80 of 86) with videos related to

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British Journal of Cancer|December 25, 2013
Germline CDH1 mutations in bilateral lobular carcinoma in situC Petridis, I Shinomiya, K Kohut, et al.
Experimental Dermatology|August 22, 2003
A Crohn's disease-associated insertion polymorphism (3020insC) in the NOD2 gene is not associated with psoriasis vulgaris, palmo-plantar pustular psoriasis or guttate psoriasisC Young, M H Allen, A Cuthbert, et al.
Diabetes|November 15, 2000
Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophyC Vigouroux, J Magré, M C Vantyghem, et al.
Molecular Genetics and Metabolism|October 1, 2011
Promoter mutation is a common variant in GJC2-associated Pelizaeus-Merzbacher-like diseaseE Meyer, M A Kurian, N V Morgan, et al.
Human Molecular Genetics|June 9, 1998
Molecular analysis of the PDS gene in Pendred syndromeB Coyle, W Reardon, J A Herbrick, et al.
Journal of Medical Genetics|January 3, 2001
Identification of a novel psoriasis susceptibility locus at 1p and evidence of epistasis between PSORS1 and candidate lociC D Veal, R L Clough, R C Barber, et al.
Journal of Medical Genetics|June 3, 2004
Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypesM A Aldred, R O C Sanford, N S Thomas, et al.
Clinical Radiology|May 19, 1998
Radiological malformations of the ear in Pendred syndromeP D Phelps, R A Coffey, R C Trembath, et al.
The New England Journal of Medicine|August 4, 2001
Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasiaR C Trembath, J R Thomson, R D Machado, et al.
Journal of Medical Genetics|June 17, 2003
A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13N V Morgan, C Bacchelli, P Gissen, et al.
Pageof 9

Showing results (71-80 of 86) with videos related to

Sort By:
Pageof 9
British Journal of Cancer|December 25, 2013
Germline CDH1 mutations in bilateral lobular carcinoma in situC Petridis, I Shinomiya, K Kohut, et al.
Experimental Dermatology|August 22, 2003
A Crohn's disease-associated insertion polymorphism (3020insC) in the NOD2 gene is not associated with psoriasis vulgaris, palmo-plantar pustular psoriasis or guttate psoriasisC Young, M H Allen, A Cuthbert, et al.
Diabetes|November 15, 2000
Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophyC Vigouroux, J Magré, M C Vantyghem, et al.
Molecular Genetics and Metabolism|October 1, 2011
Promoter mutation is a common variant in GJC2-associated Pelizaeus-Merzbacher-like diseaseE Meyer, M A Kurian, N V Morgan, et al.
Human Molecular Genetics|June 9, 1998
Molecular analysis of the PDS gene in Pendred syndromeB Coyle, W Reardon, J A Herbrick, et al.
Journal of Medical Genetics|January 3, 2001
Identification of a novel psoriasis susceptibility locus at 1p and evidence of epistasis between PSORS1 and candidate lociC D Veal, R L Clough, R C Barber, et al.
Journal of Medical Genetics|June 3, 2004
Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypesM A Aldred, R O C Sanford, N S Thomas, et al.
Clinical Radiology|May 19, 1998
Radiological malformations of the ear in Pendred syndromeP D Phelps, R A Coffey, R C Trembath, et al.
The New England Journal of Medicine|August 4, 2001
Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasiaR C Trembath, J R Thomson, R D Machado, et al.
Journal of Medical Genetics|June 17, 2003
A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13N V Morgan, C Bacchelli, P Gissen, et al.
Pageof 9