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Journal of Medical Genetics
|
February 6, 2004
A study of gene--environment interaction on the gene for angiotensin converting enzyme: a combined functional and population based approach
F A Sayed-Tabatabaei, A F C Schut, A Hofman, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
May 23, 2013
[Patients with aneurysms and osteoarthritis: Marfan syndrome ruled out, so what is it?]
Denise van der Linde, Ingrid M B H van de Laar, Adriaan Moelker, et al.
Journal of Medical Genetics
|
January 7, 2005
Angiotensin converting enzyme gene polymorphism and cardiovascular morbidity and mortality: the Rotterdam Study
F A Sayed-Tabatabaei, A F C Schut, A Arias Vásquez, et al.
Orphanet Journal of Rare Diseases
|
January 3, 2012
Congenital dyserythropoietic anemia type II: molecular analysis and expression of the SEC23B gene
Francesca Punzo, Aida M Bertoli-Avella, Saverio Scianguetta, et al.
Lupus
|
September 19, 2009
Factors associated with arterial vascular events in PROFILE: a Multiethnic Lupus Cohort
A M Bertoli, L M Vilá, G S Alarcón, et al.
Neurogenetics
|
April 28, 2009
A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier?
Esther Brusse, Danielle Majoor-Krakauer, Bianca M de Graaf, et al.
Leukemia Research
|
January 1, 1987
Abnormal splenic megakaryopoiesis in MPSV-induced myeloproliferative disease
M C Le Bousse-Kerdiles, R Fernandez-Delgado, F Smadja-Joffe, et al.
Journal of Clinical Rheumatology : Practical Reports on Rheumatic & Musculoskeletal Diseases
|
October 9, 2007
Systemic lupus erythematosus in a multiethnic US cohort (LUMINA L II): relationship between vascular events and the use of hormone replacement therapy in postmenopausal women
Mónica Fernández, Jaime Calvo-Alén, Ana M Bertoli, et al.
Clinical Genetics
|
December 23, 2020
Biallelic loss-of-function HACD1 variants are a bona fide cause of congenital myopathy
Lia Abbasi-Moheb, Ana Westenberger, Maha Alotaibi, et al.
Neurobiology of Aging
|
May 27, 2005
ACE gene is associated with Alzheimer's disease and atrophy of hippocampus and amygdala
Kristel Sleegers, Tom den Heijer, Ewoud J van Dijk, et al.
Page
of 17
Search research articles
Search
Showing results (71-80 of 168) with videos related to
Sort By:
Page
of 17
Journal of Medical Genetics
|
February 6, 2004
A study of gene--environment interaction on the gene for angiotensin converting enzyme: a combined functional and population based approach
F A Sayed-Tabatabaei, A F C Schut, A Hofman, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
May 23, 2013
[Patients with aneurysms and osteoarthritis: Marfan syndrome ruled out, so what is it?]
Denise van der Linde, Ingrid M B H van de Laar, Adriaan Moelker, et al.
Journal of Medical Genetics
|
January 7, 2005
Angiotensin converting enzyme gene polymorphism and cardiovascular morbidity and mortality: the Rotterdam Study
F A Sayed-Tabatabaei, A F C Schut, A Arias Vásquez, et al.
Orphanet Journal of Rare Diseases
|
January 3, 2012
Congenital dyserythropoietic anemia type II: molecular analysis and expression of the SEC23B gene
Francesca Punzo, Aida M Bertoli-Avella, Saverio Scianguetta, et al.
Lupus
|
September 19, 2009
Factors associated with arterial vascular events in PROFILE: a Multiethnic Lupus Cohort
A M Bertoli, L M Vilá, G S Alarcón, et al.
Neurogenetics
|
April 28, 2009
A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier?
Esther Brusse, Danielle Majoor-Krakauer, Bianca M de Graaf, et al.
Leukemia Research
|
January 1, 1987
Abnormal splenic megakaryopoiesis in MPSV-induced myeloproliferative disease
M C Le Bousse-Kerdiles, R Fernandez-Delgado, F Smadja-Joffe, et al.
Journal of Clinical Rheumatology : Practical Reports on Rheumatic & Musculoskeletal Diseases
|
October 9, 2007
Systemic lupus erythematosus in a multiethnic US cohort (LUMINA L II): relationship between vascular events and the use of hormone replacement therapy in postmenopausal women
Mónica Fernández, Jaime Calvo-Alén, Ana M Bertoli, et al.
Clinical Genetics
|
December 23, 2020
Biallelic loss-of-function HACD1 variants are a bona fide cause of congenital myopathy
Lia Abbasi-Moheb, Ana Westenberger, Maha Alotaibi, et al.
Neurobiology of Aging
|
May 27, 2005
ACE gene is associated with Alzheimer's disease and atrophy of hippocampus and amygdala
Kristel Sleegers, Tom den Heijer, Ewoud J van Dijk, et al.
Page
of 17