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W P Robinson

Showing results (81-90 of 115) with videos related to

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European Journal of Human Genetics : EJHG|December 31, 1997
Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidyA Schinzel, D Kotzot, L Brecevic, et al.
Prenatal Diagnosis|September 1, 1996
Cytogenetic and age-dependent risk factors associated with uniparental disomy 15W P Robinson, S Langlois, S Schuffenhauer, et al.
Arthritis and Rheumatism|September 1, 1989
HLA-Bw60 increases susceptibility to ankylosing spondylitis in HLA-B27+ patientsW P Robinson, S M van der Linden, M A Khan, et al.
Human Molecular Genetics|September 1, 1993
Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patientsC C Glenn, R D Nicholls, W P Robinson, et al.
Molecular Human Reproduction|December 16, 2014
Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variantsI Filges, I Manokhina, M S Peñaherrera, et al.
American Journal of Human Genetics|September 1, 1993
Nondisjunction of chromosome 15: origin and recombinationW P Robinson, F Bernasconi, A Mutirangura, et al.
Clinical Genetics|May 29, 2010
The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disordersD K Bourque, M S Peñaherrera, R K C Yuen, et al.
Journal of Medical Genetics|May 15, 1998
The mechanisms involved in formation of deletions and duplications of 15q11-q13W P Robinson, F Dutly, R D Nicholls, et al.
European Journal of Pediatrics|June 1, 1995
Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locusD Kotzot, F Bernasconi, L Brecevic, et al.
American Journal of Medical Genetics|May 15, 1994
Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?A Bottani, W P Robinson, C D DeLozier-Blanchet, et al.
Pageof 12

Showing results (81-90 of 115) with videos related to

Sort By:
Pageof 12
European Journal of Human Genetics : EJHG|December 31, 1997
Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidyA Schinzel, D Kotzot, L Brecevic, et al.
Prenatal Diagnosis|September 1, 1996
Cytogenetic and age-dependent risk factors associated with uniparental disomy 15W P Robinson, S Langlois, S Schuffenhauer, et al.
Arthritis and Rheumatism|September 1, 1989
HLA-Bw60 increases susceptibility to ankylosing spondylitis in HLA-B27+ patientsW P Robinson, S M van der Linden, M A Khan, et al.
Human Molecular Genetics|September 1, 1993
Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patientsC C Glenn, R D Nicholls, W P Robinson, et al.
Molecular Human Reproduction|December 16, 2014
Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variantsI Filges, I Manokhina, M S Peñaherrera, et al.
American Journal of Human Genetics|September 1, 1993
Nondisjunction of chromosome 15: origin and recombinationW P Robinson, F Bernasconi, A Mutirangura, et al.
Clinical Genetics|May 29, 2010
The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disordersD K Bourque, M S Peñaherrera, R K C Yuen, et al.
Journal of Medical Genetics|May 15, 1998
The mechanisms involved in formation of deletions and duplications of 15q11-q13W P Robinson, F Dutly, R D Nicholls, et al.
European Journal of Pediatrics|June 1, 1995
Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locusD Kotzot, F Bernasconi, L Brecevic, et al.
American Journal of Medical Genetics|May 15, 1994
Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?A Bottani, W P Robinson, C D DeLozier-Blanchet, et al.
Pageof 12