A de Paepe - JoVE Visualize

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BJU International|June 26, 2002

Does monosymptomatic enuresis exist? A molecular genetic exploration of 32 families with enuresis/incontinenceB Loeys, P Hoebeke, A Raes, et al.

Archives of Oral Biology|November 23, 2006

Abnormal dentin structure in two novel gene mutations [COL1A1, Arg134Cys] and [ADAMTS2, Trp795-to-ter] causing rare type I collagen disordersP J De Coster, M Cornelissen, A De Paepe, et al.

European Journal of Human Genetics : EJHG|May 1, 1997

Osteogenesis imperfecta phenotypes resulting from serine for glycine substitutions in the alpha2(I) collagen chainL Nuytinck, K Wettinck, M Freund, et al.

Clinical Genetics|August 28, 2007

Utility of molecular analyses in the exploration of extreme intrafamilial variability in the Marfan syndromeJ De Backer, B Loeys, B Leroy, et al.

Human Reproduction (Oxford, England)|April 1, 1997

Triple colour fluorescent in-situ hybridization for chromosomes X,Y and 1 on spare human embryosH Laverge, P De Sutter, M R Verschraegen-Spae, et al.

Human Mutation|March 25, 1999

Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease. Mutations in brief no. 224. OnlineK Claes, E Machackova, M De Vos, et al.

Prenatal Diagnosis|May 1, 1993

Molecular cytogenetic characterization of marker chromosomes found at prenatal diagnosisM R Verschraegen-Spae, N van Roy, A de Perdigo, et al.

Human Genetics|November 1, 1994

Three unrelated individuals with perinatally lethal osteogenesis imperfecta resulting from identical Gly502Ser substitutions in the alpha 2-chain of type I collagenN J Rose, K Mackay, A De Paepe, et al.

Methods in Cell Biology|July 23, 2016

RT-qPCR gene expression analysis in zebrafish: Preanalytical precautions and use of expressed repetitive elements for normalizationS Vanhauwaert, S Lefever, P Coucke, et al.

American Journal of Human Genetics|March 31, 2000

Classical Ehlers-Danlos syndrome caused by a mutation in type I collagenL Nuytinck, M Freund, L Lagae, et al.

Pageof 15

Showing results (51-60 of 142) with videos related to

Sort By:

Pageof 15

BJU International|June 26, 2002

Does monosymptomatic enuresis exist? A molecular genetic exploration of 32 families with enuresis/incontinenceB Loeys, P Hoebeke, A Raes, et al.

Archives of Oral Biology|November 23, 2006

Abnormal dentin structure in two novel gene mutations [COL1A1, Arg134Cys] and [ADAMTS2, Trp795-to-ter] causing rare type I collagen disordersP J De Coster, M Cornelissen, A De Paepe, et al.

European Journal of Human Genetics : EJHG|May 1, 1997

Osteogenesis imperfecta phenotypes resulting from serine for glycine substitutions in the alpha2(I) collagen chainL Nuytinck, K Wettinck, M Freund, et al.

Clinical Genetics|August 28, 2007

Utility of molecular analyses in the exploration of extreme intrafamilial variability in the Marfan syndromeJ De Backer, B Loeys, B Leroy, et al.

Human Reproduction (Oxford, England)|April 1, 1997

Triple colour fluorescent in-situ hybridization for chromosomes X,Y and 1 on spare human embryosH Laverge, P De Sutter, M R Verschraegen-Spae, et al.

Human Mutation|March 25, 1999

Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease. Mutations in brief no. 224. OnlineK Claes, E Machackova, M De Vos, et al.

Prenatal Diagnosis|May 1, 1993

Molecular cytogenetic characterization of marker chromosomes found at prenatal diagnosisM R Verschraegen-Spae, N van Roy, A de Perdigo, et al.

Human Genetics|November 1, 1994

Three unrelated individuals with perinatally lethal osteogenesis imperfecta resulting from identical Gly502Ser substitutions in the alpha 2-chain of type I collagenN J Rose, K Mackay, A De Paepe, et al.

Methods in Cell Biology|July 23, 2016

RT-qPCR gene expression analysis in zebrafish: Preanalytical precautions and use of expressed repetitive elements for normalizationS Vanhauwaert, S Lefever, P Coucke, et al.

American Journal of Human Genetics|March 31, 2000

Classical Ehlers-Danlos syndrome caused by a mutation in type I collagenL Nuytinck, M Freund, L Lagae, et al.

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