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A DE Paepe

Showing results (31-40 of 173) with videos related to

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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.
Genetic Counseling (Geneva, Switzerland)|August 5, 2010
A Turkish patient of typical Loeys-Dietz syndrome with a TGFBR2 mutationE Tug, B Loeys, A De Paepe, et al.
Journal De Genetique Humaine|June 1, 1988
[The Ehlers-Danlos and Marfan syndromes in young children]A De Paepe, H Van den Bossche, G Mortier, et al.
Human Mutation|January 1, 1995
Substitution of valine for glycine 793 in type III procollagen in Ehlers-Danlos syndrome type IVG Tromp, A De Paepe, L Nuytinck, et al.
Human Genetics|January 7, 1998
Characterisation of two different nonsense mutations, C6792A and C6792G, causing skipping of exon 37 in the NF1 geneL Messiaen, T Callens, A De Paepe, et al.
Human Mutation|January 1, 1994
Single-strand conformation polymorphism (SSCP) analysis of the COL3A1 gene detects a mutation that results in the substitution of glycine 1009 to valine and causes severe Ehlers-Danlos syndrome type IVL Nuytinck, A De Paepe, J P Renard, et al.
Clinical Neurology and Neurosurgery|January 1, 1988
Association of multiple intracranial aneurysms and collagen type III deficiencyA de Paepe, W van Landegem, F de Keyser, et al.
Acta Gastro-Enterologica Belgica|February 24, 2001
Prevalence of the Cys282Tyr and His63Asp mutation in Flemish patients with hereditary hemochromatosisH Van Vlierberghe, L Messiaen, M Hautekeete, et al.
American Journal of Medical Genetics|January 1, 1993
Osteoporosis-pseudoglioma syndromeA De Paepe, J G Leroy, L Nuytinck, et al.
Pageof 18

Showing results (31-40 of 173) with videos related to

Sort By:
Pageof 18
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.
Genetic Counseling (Geneva, Switzerland)|August 5, 2010
A Turkish patient of typical Loeys-Dietz syndrome with a TGFBR2 mutationE Tug, B Loeys, A De Paepe, et al.
Journal De Genetique Humaine|June 1, 1988
[The Ehlers-Danlos and Marfan syndromes in young children]A De Paepe, H Van den Bossche, G Mortier, et al.
Human Mutation|January 1, 1995
Substitution of valine for glycine 793 in type III procollagen in Ehlers-Danlos syndrome type IVG Tromp, A De Paepe, L Nuytinck, et al.
Human Genetics|January 7, 1998
Characterisation of two different nonsense mutations, C6792A and C6792G, causing skipping of exon 37 in the NF1 geneL Messiaen, T Callens, A De Paepe, et al.
Human Mutation|January 1, 1994
Single-strand conformation polymorphism (SSCP) analysis of the COL3A1 gene detects a mutation that results in the substitution of glycine 1009 to valine and causes severe Ehlers-Danlos syndrome type IVL Nuytinck, A De Paepe, J P Renard, et al.
Clinical Neurology and Neurosurgery|January 1, 1988
Association of multiple intracranial aneurysms and collagen type III deficiencyA de Paepe, W van Landegem, F de Keyser, et al.
Acta Gastro-Enterologica Belgica|February 24, 2001
Prevalence of the Cys282Tyr and His63Asp mutation in Flemish patients with hereditary hemochromatosisH Van Vlierberghe, L Messiaen, M Hautekeete, et al.
American Journal of Medical Genetics|January 1, 1993
Osteoporosis-pseudoglioma syndromeA De Paepe, J G Leroy, L Nuytinck, et al.
Pageof 18