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Journal of Medical Genetics
|
July 2, 2010
The revised Ghent nosology for the Marfan syndrome
Bart L Loeys, Harry C Dietz, Alan C Braverman, et al.
European Journal of Human Genetics : EJHG
|
April 15, 2010
Altered TGFbeta signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency
Marjolijn Renard, Tammy Holm, Regan Veith, et al.
Orphanet Journal of Rare Diseases
|
December 31, 2011
Osteogenesis Imperfecta: the audiological phenotype lacks correlation with the genotype
Freya K R Swinnen, Paul J Coucke, Anne M De Paepe, et al.
Human Mutation
|
November 14, 2008
Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature
Bert L Callewaert, Bart L Loeys, Anna Ficcadenti, et al.
The New England Journal of Medicine
|
August 25, 2006
Aneurysm syndromes caused by mutations in the TGF-beta receptor
Bart L Loeys, Ulrike Schwarze, Tammy Holm, et al.
Human Mutation
|
October 16, 2007
Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families
B L Callewaert, A Willaert, W S Kerstjens-Frederikse, et al.
Nature Genetics
|
February 26, 2005
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
Bart L Loeys, Junji Chen, Enid R Neptune, et al.
American Heart Journal
|
May 13, 2015
Design and rationale of a prospective, collaborative meta-analysis of all randomized controlled trials of angiotensin receptor antagonists in Marfan syndrome, based on individual patient data: A report from the Marfan Treatment Trialists' Collaboration
Alex Pitcher, Jonathan Emberson, Ronald V Lacro, et al.
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Search research articles
Search
Showing results (41-50 of 48) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 48 results.
Journal of Medical Genetics
|
July 2, 2010
The revised Ghent nosology for the Marfan syndrome
Bart L Loeys, Harry C Dietz, Alan C Braverman, et al.
European Journal of Human Genetics : EJHG
|
April 15, 2010
Altered TGFbeta signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency
Marjolijn Renard, Tammy Holm, Regan Veith, et al.
Orphanet Journal of Rare Diseases
|
December 31, 2011
Osteogenesis Imperfecta: the audiological phenotype lacks correlation with the genotype
Freya K R Swinnen, Paul J Coucke, Anne M De Paepe, et al.
Human Mutation
|
November 14, 2008
Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature
Bert L Callewaert, Bart L Loeys, Anna Ficcadenti, et al.
The New England Journal of Medicine
|
August 25, 2006
Aneurysm syndromes caused by mutations in the TGF-beta receptor
Bart L Loeys, Ulrike Schwarze, Tammy Holm, et al.
Human Mutation
|
October 16, 2007
Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families
B L Callewaert, A Willaert, W S Kerstjens-Frederikse, et al.
Nature Genetics
|
February 26, 2005
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
Bart L Loeys, Junji Chen, Enid R Neptune, et al.
American Heart Journal
|
May 13, 2015
Design and rationale of a prospective, collaborative meta-analysis of all randomized controlled trials of angiotensin receptor antagonists in Marfan syndrome, based on individual patient data: A report from the Marfan Treatment Trialists' Collaboration
Alex Pitcher, Jonathan Emberson, Ronald V Lacro, et al.
Page
of 5