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A C J Gijsbers

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Cytogenetic and Genome Research|November 17, 2011
Interpretation of array comparative genome hybridization data: a major challengeA C J Gijsbers, J Schoumans, C A L Ruivenkamp
Hormone Research in Paediatrics|April 10, 2014
Pseudoisodicentric Xp chromosome [46,X,psu idic(X)(q21.1)] and its effect on growth and pubertal developmentH J van der Kamp, S G Kant, C A L Ruivenkamp, et al.
Cytogenetic and Genome Research|May 1, 2010
A subtle familial translocation t(3;21)(p26.3;q22.3): an apparently healthy boy with a 3p deletion and 21q duplicationA C J Gijsbers, A van Haeringen, C A J Bosch, et al.
Journal of Medical Genetics|February 28, 2009
A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parentsJ Knijnenburg, S A J Lesnik Oberstein, K Frei, et al.
Journal of Intellectual Disability Research : JIDR|March 7, 2017
Estimates of live birth prevalence of children with Down syndrome in the period 1991-2015 in the NetherlandsG de Graaf, J J M Engelen, A C J Gijsbers, et al.
Clinical Genetics|May 22, 2010
X-chromosome duplications in males with mental retardation: pathogenic or benign variants?A C J Gijsbers, N S den Hollander, A T J M Helderman-van de Enden, et al.
American Journal of Human Genetics|February 29, 2008
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profilesCarl E G Bruder, Arkadiusz Piotrowski, Antoinet A C J Gijsbers, et al.
Hormone Research in Paediatrics|June 9, 2012
Genetic analysis of short children with apparent growth hormone insensitivityJ M Wit, H A van Duyvenvoorde, S A Scheltinga, et al.
European Journal of Medical Genetics|April 24, 2012
Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardationE K Bijlsma, A Collins, F T Papa, et al.
European Journal of Medical Genetics|March 25, 2009
Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individualsE K Bijlsma, A C J Gijsbers, J H M Schuurs-Hoeijmakers, et al.
Pageof 1

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

Sort By:
Pageof 1
Cytogenetic and Genome Research|November 17, 2011
Interpretation of array comparative genome hybridization data: a major challengeA C J Gijsbers, J Schoumans, C A L Ruivenkamp
Hormone Research in Paediatrics|April 10, 2014
Pseudoisodicentric Xp chromosome [46,X,psu idic(X)(q21.1)] and its effect on growth and pubertal developmentH J van der Kamp, S G Kant, C A L Ruivenkamp, et al.
Cytogenetic and Genome Research|May 1, 2010
A subtle familial translocation t(3;21)(p26.3;q22.3): an apparently healthy boy with a 3p deletion and 21q duplicationA C J Gijsbers, A van Haeringen, C A J Bosch, et al.
Journal of Medical Genetics|February 28, 2009
A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parentsJ Knijnenburg, S A J Lesnik Oberstein, K Frei, et al.
Journal of Intellectual Disability Research : JIDR|March 7, 2017
Estimates of live birth prevalence of children with Down syndrome in the period 1991-2015 in the NetherlandsG de Graaf, J J M Engelen, A C J Gijsbers, et al.
Clinical Genetics|May 22, 2010
X-chromosome duplications in males with mental retardation: pathogenic or benign variants?A C J Gijsbers, N S den Hollander, A T J M Helderman-van de Enden, et al.
American Journal of Human Genetics|February 29, 2008
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profilesCarl E G Bruder, Arkadiusz Piotrowski, Antoinet A C J Gijsbers, et al.
Hormone Research in Paediatrics|June 9, 2012
Genetic analysis of short children with apparent growth hormone insensitivityJ M Wit, H A van Duyvenvoorde, S A Scheltinga, et al.
European Journal of Medical Genetics|April 24, 2012
Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardationE K Bijlsma, A Collins, F T Papa, et al.
European Journal of Medical Genetics|March 25, 2009
Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individualsE K Bijlsma, A C J Gijsbers, J H M Schuurs-Hoeijmakers, et al.
Pageof 1