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Human Molecular Genetics
|
September 15, 1999
Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis
G C Black, R Perveen, R Bonshek, et al.
Mymensingh Medical Journal : MMJ
|
December 7, 2017
Assessment of Subvalvular Apparatus in Patients with Rheumatic Mitral Stenosis: Comparison between 2D and 3D Echocardiography
S S Shakil, C M Ahmed, F I Khaled, et al.
American Journal of Human Genetics
|
August 1, 1994
A YAC contig encompassing the Treacher Collins syndrome critical region at 5q31.3-32
J Dixon, A J Gladwin, S K Loftus, et al.
Genomics
|
April 13, 1999
Refined genetic and physical localization of the Wagner disease (WGN1) locus and the genes CRTL1 and CSPG2 to a 2- to 2.5-cM region of chromosome 5q14.3
R Perveen, N Hart-Holden, M J Dixon, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society
|
October 27, 2018
Mode of presentation and mortality amongst patients hospitalized with heart failure? A report from the First Euro Heart Failure Survey
Ahmad Shoaib, M Farag, J Nolan, et al.
Investigative Ophthalmology & Visual Science
|
August 11, 2000
Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations
R Perveen, I C Lloyd, J Clayton-Smith, et al.
Mymensingh Medical Journal : MMJ
|
August 25, 2018
An Echocardiographic Study of the Right Ventricular Diastolic Function in Systemic Hypertension and Its Relation with the Left Ventricular Homologous Changes
R Perveen, M H Hoque, K Ahmed, et al.
Investigative Ophthalmology & Visual Science
|
September 28, 2000
Ultrastructural and molecular analysis of Bowman's layer corneal dystrophies: an epithelial origin?
A E Ridgway, S Akhtar, F L Munier, et al.
Human Molecular Genetics
|
November 2, 2001
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy
S Biswas, F L Munier, J Yardley, et al.
Journal of Medical Genetics
|
January 31, 2006
Genotype-phenotype correlation in Costello syndrome: HRAS mutation analysis in 43 cases
B Kerr, M-A Delrue, S Sigaudy, et al.
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Search research articles
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Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Human Molecular Genetics
|
September 15, 1999
Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis
G C Black, R Perveen, R Bonshek, et al.
Mymensingh Medical Journal : MMJ
|
December 7, 2017
Assessment of Subvalvular Apparatus in Patients with Rheumatic Mitral Stenosis: Comparison between 2D and 3D Echocardiography
S S Shakil, C M Ahmed, F I Khaled, et al.
American Journal of Human Genetics
|
August 1, 1994
A YAC contig encompassing the Treacher Collins syndrome critical region at 5q31.3-32
J Dixon, A J Gladwin, S K Loftus, et al.
Genomics
|
April 13, 1999
Refined genetic and physical localization of the Wagner disease (WGN1) locus and the genes CRTL1 and CSPG2 to a 2- to 2.5-cM region of chromosome 5q14.3
R Perveen, N Hart-Holden, M J Dixon, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society
|
October 27, 2018
Mode of presentation and mortality amongst patients hospitalized with heart failure? A report from the First Euro Heart Failure Survey
Ahmad Shoaib, M Farag, J Nolan, et al.
Investigative Ophthalmology & Visual Science
|
August 11, 2000
Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations
R Perveen, I C Lloyd, J Clayton-Smith, et al.
Mymensingh Medical Journal : MMJ
|
August 25, 2018
An Echocardiographic Study of the Right Ventricular Diastolic Function in Systemic Hypertension and Its Relation with the Left Ventricular Homologous Changes
R Perveen, M H Hoque, K Ahmed, et al.
Investigative Ophthalmology & Visual Science
|
September 28, 2000
Ultrastructural and molecular analysis of Bowman's layer corneal dystrophies: an epithelial origin?
A E Ridgway, S Akhtar, F L Munier, et al.
Human Molecular Genetics
|
November 2, 2001
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy
S Biswas, F L Munier, J Yardley, et al.
Journal of Medical Genetics
|
January 31, 2006
Genotype-phenotype correlation in Costello syndrome: HRAS mutation analysis in 43 cases
B Kerr, M-A Delrue, S Sigaudy, et al.
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of 2