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W Nillesen

Showing results (1-10 of 10) with videos related to

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Human Molecular Genetics|March 1, 1993
Dinucleotide repeat polymorphism at locus D19S207, close to the myotonic dystrophy (DM) geneG Jansen, M Coerwinkel-Driessen, W Nillesen, et al.
American Journal of Human Genetics|April 1, 1994
Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in spermG Jansen, P Willems, M Coerwinkel, et al.
Journal of Medical Genetics|November 1, 1992
Presymptomatic diagnosis of myotonic dystrophyH G Brunner, W Nillesen, B A van Oost, et al.
Molecular Syndromology|July 26, 2013
Noonan syndrome: comparing mutation-positive with mutation-negative dutch patientsE A Croonen, W Nillesen, C Schrander, et al.
The New England Journal of Medicine|February 18, 1993
Brief report: reverse mutation in myotonic dystrophyH G Brunner, G Jansen, W Nillesen, et al.
American Journal of Human Genetics|November 1, 1993
Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)H G Brunner, H T Brüggenwirth, W Nillesen, et al.
Brain : a Journal of Neurology|October 1, 1991
Myotonic dystrophy. Predictive value of normal results on clinical examinationH G Brunner, H J Smeets, W Nillesen, et al.
Journal of Medical Genetics|February 5, 2008
A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysisN de Leeuw, R Pfundt, D A Koolen, et al.
Clinical Genetics|April 22, 2004
A novel microdeletion, del(2)(q22.3q23.3) in a mentally retarded patient, detected by array-based comparative genomic hybridizationD A Koolen, L E L M Vissers, W Nillesen, et al.
Journal of Medical Genetics|April 5, 2005
Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndromeT Kleefstra, M Smidt, M J G Banning, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Human Molecular Genetics|March 1, 1993
Dinucleotide repeat polymorphism at locus D19S207, close to the myotonic dystrophy (DM) geneG Jansen, M Coerwinkel-Driessen, W Nillesen, et al.
American Journal of Human Genetics|April 1, 1994
Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in spermG Jansen, P Willems, M Coerwinkel, et al.
Journal of Medical Genetics|November 1, 1992
Presymptomatic diagnosis of myotonic dystrophyH G Brunner, W Nillesen, B A van Oost, et al.
Molecular Syndromology|July 26, 2013
Noonan syndrome: comparing mutation-positive with mutation-negative dutch patientsE A Croonen, W Nillesen, C Schrander, et al.
The New England Journal of Medicine|February 18, 1993
Brief report: reverse mutation in myotonic dystrophyH G Brunner, G Jansen, W Nillesen, et al.
American Journal of Human Genetics|November 1, 1993
Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)H G Brunner, H T Brüggenwirth, W Nillesen, et al.
Brain : a Journal of Neurology|October 1, 1991
Myotonic dystrophy. Predictive value of normal results on clinical examinationH G Brunner, H J Smeets, W Nillesen, et al.
Journal of Medical Genetics|February 5, 2008
A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysisN de Leeuw, R Pfundt, D A Koolen, et al.
Clinical Genetics|April 22, 2004
A novel microdeletion, del(2)(q22.3q23.3) in a mentally retarded patient, detected by array-based comparative genomic hybridizationD A Koolen, L E L M Vissers, W Nillesen, et al.
Journal of Medical Genetics|April 5, 2005
Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndromeT Kleefstra, M Smidt, M J G Banning, et al.
Pageof 1