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The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation
|
March 16, 2001
Mutations in the TGF-beta type 1 receptor, ALK1, in combined primary pulmonary hypertension and hereditary haemorrhagic telangiectasia, implies pathway specificity
R C. Trembath
Journal of the Royal College of Physicians of London
|
March 1, 1994
Genetic mechanisms and mental retardation
R C Trembath
Journal of Medical Genetics
|
December 1, 1996
Pendred syndrome
W Reardon, R C Trembath
The European Respiratory Journal
|
October 3, 2002
Genetics of pulmonary hypertension: from bench to bedside
M Humbert, R C Trembath
Human Mutation
|
September 12, 2000
Activating and inactivating mutations in the human GNAS1 gene
M A Aldred, R C Trembath
Journal of Medical Genetics
|
October 1, 1994
Albright's hereditary osteodystrophy
L C Wilson, R C Trembath
Biomedica Biochimica Acta
|
January 1, 1988
Genetic variants of the insulin receptor in type II (non-insulin dependent) diabetes mellitus
D J Galton, R C Trembath
Nucleic Acids Research
|
April 13, 2005
A dual-light reporter system to determine the efficiency of protein-protein interactions in mammalian cells
M T Nasim, R C Trembath
Journal of Clinical Pathology
|
March 27, 2001
Primary pulmonary hypertension: the pressure rises for a gene
J R Thomson, R C Trembath
The British Journal of Dermatology
|
January 1, 1997
Genetic studies of atopy and atopic dermatitis
R Coleman, R C Trembath, J I Harper
Page
of 9
Search research articles
Search
Showing results (1-10 of 86) with videos related to
Sort By:
Page
of 9
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation
|
March 16, 2001
Mutations in the TGF-beta type 1 receptor, ALK1, in combined primary pulmonary hypertension and hereditary haemorrhagic telangiectasia, implies pathway specificity
R C. Trembath
Journal of the Royal College of Physicians of London
|
March 1, 1994
Genetic mechanisms and mental retardation
R C Trembath
Journal of Medical Genetics
|
December 1, 1996
Pendred syndrome
W Reardon, R C Trembath
The European Respiratory Journal
|
October 3, 2002
Genetics of pulmonary hypertension: from bench to bedside
M Humbert, R C Trembath
Human Mutation
|
September 12, 2000
Activating and inactivating mutations in the human GNAS1 gene
M A Aldred, R C Trembath
Journal of Medical Genetics
|
October 1, 1994
Albright's hereditary osteodystrophy
L C Wilson, R C Trembath
Biomedica Biochimica Acta
|
January 1, 1988
Genetic variants of the insulin receptor in type II (non-insulin dependent) diabetes mellitus
D J Galton, R C Trembath
Nucleic Acids Research
|
April 13, 2005
A dual-light reporter system to determine the efficiency of protein-protein interactions in mammalian cells
M T Nasim, R C Trembath
Journal of Clinical Pathology
|
March 27, 2001
Primary pulmonary hypertension: the pressure rises for a gene
J R Thomson, R C Trembath
The British Journal of Dermatology
|
January 1, 1997
Genetic studies of atopy and atopic dermatitis
R Coleman, R C Trembath, J I Harper
Page
of 9