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Journal of Community Genetics|January 1, 2013
Attitudes of health care professionals toward carrier screening for cystic fibrosis. A review of the literatureS Janssens, A De Paepe, P BorryClinical Genetics|February 1, 1996
Neuropsychological aspects of Marfan syndromeE Lannoo, A De Paepe, B Leroy, et al.Prenatal Diagnosis|October 16, 1999
Prenatal diagnosis of osteogenesis imperfecta type I by COL1A1 null-allele testingL Nuytinck, B S Sayli, W Karen, et al.Fetal Diagnosis and Therapy|July 27, 1999
Preterm premature rupture of membranes in a patient with the hypermobility type of the Ehlers-Danlos syndrome. A case reportM De Vos, L Nuytinck, C Verellen, et al.International Angiology : a Journal of the International Union of Angiology|January 1, 1986
Pulse wave velocity recordings in a family with ecchymotic Ehlers-Danlos syndromeB François, A De Paepe, M T Matton, et al.Clinical Dysmorphology|August 24, 1999
Occipital Horn syndrome in a 2-year-old boyA De Paepe, B Loeys, K Devriendt, et al.Human Genetics|April 1, 1997
Homozygosity by descent for a COL1A2 mutation in two sibs with severe osteogenesis imperfecta and mild clinical expression in the heterozygotesA De Paepe, L Nuytinck, M Raes, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|July 2, 2010
Vascular haemostasisN S Key, A DE Paepe, F Malfait, et al.British Journal of Cancer|March 18, 2004
BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer familiesK Claes, B Poppe, I Coene, et al.Progress in Clinical and Biological Research|January 1, 1982
Unusual familial manifestation of Ehlers-Danlos syndromeM T Matton, A De Paepe, F De Keyser, et al.Pageof 15