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A J Verkerk

Showing results (1-10 of 22) with videos related to

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Chromosoma|April 1, 1992
The fragile X syndrome: isolation of the FMR-1 gene and characterization of the fragile X mutationB A Oostra, A J Verkerk
American Journal of Medical Genetics|April 1, 1992
Limited size of the fragile X site shown by fluorescence in situ hybridizationA J Verkerk, B H Eussen, J O Van Hemel, et al.
American Journal of Human Genetics|April 17, 1999
Heterogeneous X inactivation in trophoblastic cells of human full-term female placentasL H Looijenga, A J Gillis, A J Verkerk, et al.
The American Journal of Pathology|August 1, 1997
X inactivation in human testicular tumors. XIST expression and androgen receptor methylation statusL H Looijenga, A J Gillis, R J van Gurp, et al.
British Journal of Cancer|January 1, 1997
Methylation similarities of two CpG sites within exon 5 of human H19 between normal tissues and testicular germ cell tumours of adolescents and adults, without correlation with allelic and total level of expressionA J Gillis, A J Verkerk, M C Dekker, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|April 3, 1998
Genomic imprinting in testicular germ cell tumoursL H Looijenga, A J Verkerk, M C Dekker, et al.
Journal of Clinical Periodontology|January 12, 2005
Three different rinsing times and inhibition of plaque accumulation with chlorhexidineG A Van der Weijden, M F Timmerman, A G A Novotny, et al.
Genomics|April 1, 1992
Genetic mapping on the mouse X chromosome of human cDNA clones for the fragile X and Hunter syndromesC J Faust, A J Verkerk, P J Wilson, et al.
Oncogene|October 17, 1996
Characterization of the imprinted IPW gene: allelic expression in normal and tumorigenic human tissuesJ Rachmilewitz, M Elkin, L H Looijenga, et al.
American Journal of Medical Genetics|July 15, 1994
No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndromeP Chiurazzi, E de Graaff, J Ng, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Chromosoma|April 1, 1992
The fragile X syndrome: isolation of the FMR-1 gene and characterization of the fragile X mutationB A Oostra, A J Verkerk
American Journal of Medical Genetics|April 1, 1992
Limited size of the fragile X site shown by fluorescence in situ hybridizationA J Verkerk, B H Eussen, J O Van Hemel, et al.
American Journal of Human Genetics|April 17, 1999
Heterogeneous X inactivation in trophoblastic cells of human full-term female placentasL H Looijenga, A J Gillis, A J Verkerk, et al.
The American Journal of Pathology|August 1, 1997
X inactivation in human testicular tumors. XIST expression and androgen receptor methylation statusL H Looijenga, A J Gillis, R J van Gurp, et al.
British Journal of Cancer|January 1, 1997
Methylation similarities of two CpG sites within exon 5 of human H19 between normal tissues and testicular germ cell tumours of adolescents and adults, without correlation with allelic and total level of expressionA J Gillis, A J Verkerk, M C Dekker, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|April 3, 1998
Genomic imprinting in testicular germ cell tumoursL H Looijenga, A J Verkerk, M C Dekker, et al.
Journal of Clinical Periodontology|January 12, 2005
Three different rinsing times and inhibition of plaque accumulation with chlorhexidineG A Van der Weijden, M F Timmerman, A G A Novotny, et al.
Genomics|April 1, 1992
Genetic mapping on the mouse X chromosome of human cDNA clones for the fragile X and Hunter syndromesC J Faust, A J Verkerk, P J Wilson, et al.
Oncogene|October 17, 1996
Characterization of the imprinted IPW gene: allelic expression in normal and tumorigenic human tissuesJ Rachmilewitz, M Elkin, L H Looijenga, et al.
American Journal of Medical Genetics|July 15, 1994
No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndromeP Chiurazzi, E de Graaff, J Ng, et al.
Pageof 3