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Dermatology (Basel, Switzerland)|January 1, 1994
Ehlers-Danlos syndrome type IV. Clinical and molecular aspects and guidelines for diagnosis and managementA De PaepeVerhandelingen - Koninklijke Academie Voor Geneeskunde Van Belgie|February 16, 1999
Heritable collagen disorders: from phenotype to genotypeA De PaepeClinical Genetics|February 23, 2012
The Ehlers-Danlos syndrome, a disorder with many facesA De Paepe, F MalfaitVerhandelingen - Koninklijke Academie Voor Geneeskunde Van Belgie|July 18, 2008
New insights in the pathogenesis of aortic aneurysmsB Loeys, A De PaepeGenetic Counseling (Geneva, Switzerland)|January 1, 1991
Genetic counseling of a couple presenting respectively terminal transverse defects and congenital arthrogryposisA De Paepe, S De BieInternational Journal of Pediatrics|February 13, 2013
Pharmacogenomics in children: advantages and challenges of next generation sequencing applicationsO M Vanakker, A De PaepeJournal of Medical Genetics|June 4, 1998
Psychosocial adaptation in adolescents and young adults with Marfan syndrome: an exploratory studyA Van Tongerloo, A De PaepeJournal Belge De Radiologie|August 1, 1993
The osteoporosis pseudoglioma syndromeJ Capoen, A De Paepe, H LauwersVerhandelingen - Koninklijke Academie Voor Geneeskunde Van Belgie|April 13, 2007
Acquired chromosomal rearrangements targeting selected transcription factors: contribution of molecular cytogenetic and expression analyses to the identification of clinically and biologically relevant subgroups in hematological malignanciesB Poppe, A De Paepe, F SpelemanMatrix Biology : Journal of the International Society for Matrix Biology|March 21, 1998
A four base pair insertion polymorphism in the 3' untranslated region of the COL1A1 gene is highly informative for null-allele testing in patients with osteogenesis imperfecta type IL Nuytinck, C Coppin, A De PaepePageof 15