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A DE Paepe

Showing results (21-30 of 173) with videos related to

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Human Mutation|January 1, 1994
Substitution of glycine-172 by arginine in the alpha 1 chain of type I collagen in a patient with osteogenesis imperfecta, type IIIK Mackay, A De Paepe, L Nuytinck, et al.
Clinical Genetics|February 1, 1996
Neuropsychological aspects of Marfan syndromeE Lannoo, A De Paepe, B Leroy, et al.
The British Journal of Dermatology|May 20, 2000
COL3A1 mutation leading to acrogeria (Gottron Type)T Jansen, A de Paepe, N Luytinck, 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.
Rheumatology (Oxford, England)|January 19, 2006
The genetic basis of the joint hypermobility syndromesF Malfait, A J Hakim, A De Paepe, 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.
Pageof 18

Showing results (21-30 of 173) with videos related to

Sort By:
Pageof 18
Human Mutation|January 1, 1994
Substitution of glycine-172 by arginine in the alpha 1 chain of type I collagen in a patient with osteogenesis imperfecta, type IIIK Mackay, A De Paepe, L Nuytinck, et al.
Clinical Genetics|February 1, 1996
Neuropsychological aspects of Marfan syndromeE Lannoo, A De Paepe, B Leroy, et al.
The British Journal of Dermatology|May 20, 2000
COL3A1 mutation leading to acrogeria (Gottron Type)T Jansen, A de Paepe, N Luytinck, 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.
Rheumatology (Oxford, England)|January 19, 2006
The genetic basis of the joint hypermobility syndromesF Malfait, A J Hakim, A De Paepe, 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.
Pageof 18