Search research articles
Contact Us
Filters
Showing results (1-10 of 122) with videos related to
Page
of 13
Sort By:
Advances in Experimental Medicine and Biology
|
January 21, 2014
Loeys-Dietz syndrome
Lut Van Laer, Harry Dietz, Bart Loeys
Human Genetics
|
September 12, 2008
Human hereditary hearing impairment: mouse models can help to solve the puzzle
Karen Vrijens, Lut Van Laer, Guy Van Camp
Circulation Research
|
July 23, 2013
Genetics of thoracic aortic aneurysm: at the crossroad of transforming growth factor-β signaling and vascular smooth muscle cell contractility
Elisabeth Gillis, Lut Van Laer, Bart L Loeys
Gene
|
December 20, 2008
Characterization of the murine Dfna5 promoter and regulatory regions
Karen Vrijens, Guy Van Camp, Lut Van Laer
Ear and Hearing
|
February 6, 2009
Genetic studies on noise-induced hearing loss: a review
Annelies Konings, Lut Van Laer, Guy Van Camp
Current Opinion in Pediatrics
|
June 19, 2012
Marfan syndrome: from gene to therapy
Nikhita Bolar, Lut Van Laer, Bart L Loeys
European Journal of Pediatrics
|
July 18, 2012
Educational paper. Connective tissue disorders with vascular involvement: from gene to therapy
Lut Van Laer, Dorien Proost, Bart L Loeys
Human Mutation
|
February 27, 2016
Marfan Syndrome and Related Disorders: 25 Years of Gene Discovery
Aline Verstraeten, Maaike Alaerts, Lut Van Laer, et al.
Experimental Gerontology
|
April 3, 2003
Age-related hearing impairment (ARHI): environmental risk factors and genetic prospects
Erik Fransen, Nele Lemkens, Lut Van Laer, et al.
The Annals of Otology, Rhinology, and Laryngology
|
April 26, 2012
DFNA5, a gene involved in hearing loss and cancer: a review
Ken Op de Beeck, Lut Van Laer, Guy Van Camp
Page
of 13
Search research articles
Search
Showing results (1-10 of 122) with videos related to
Sort By:
Page
of 13
Advances in Experimental Medicine and Biology
|
January 21, 2014
Loeys-Dietz syndrome
Lut Van Laer, Harry Dietz, Bart Loeys
Human Genetics
|
September 12, 2008
Human hereditary hearing impairment: mouse models can help to solve the puzzle
Karen Vrijens, Lut Van Laer, Guy Van Camp
Circulation Research
|
July 23, 2013
Genetics of thoracic aortic aneurysm: at the crossroad of transforming growth factor-β signaling and vascular smooth muscle cell contractility
Elisabeth Gillis, Lut Van Laer, Bart L Loeys
Gene
|
December 20, 2008
Characterization of the murine Dfna5 promoter and regulatory regions
Karen Vrijens, Guy Van Camp, Lut Van Laer
Ear and Hearing
|
February 6, 2009
Genetic studies on noise-induced hearing loss: a review
Annelies Konings, Lut Van Laer, Guy Van Camp
Current Opinion in Pediatrics
|
June 19, 2012
Marfan syndrome: from gene to therapy
Nikhita Bolar, Lut Van Laer, Bart L Loeys
European Journal of Pediatrics
|
July 18, 2012
Educational paper. Connective tissue disorders with vascular involvement: from gene to therapy
Lut Van Laer, Dorien Proost, Bart L Loeys
Human Mutation
|
February 27, 2016
Marfan Syndrome and Related Disorders: 25 Years of Gene Discovery
Aline Verstraeten, Maaike Alaerts, Lut Van Laer, et al.
Experimental Gerontology
|
April 3, 2003
Age-related hearing impairment (ARHI): environmental risk factors and genetic prospects
Erik Fransen, Nele Lemkens, Lut Van Laer, et al.
The Annals of Otology, Rhinology, and Laryngology
|
April 26, 2012
DFNA5, a gene involved in hearing loss and cancer: a review
Ken Op de Beeck, Lut Van Laer, Guy Van Camp
Page
of 13