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R G Mensink

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Human Molecular Genetics|November 1, 1992
Three dinucleotide repeat polymorphisms at the DXS178 locusM de Weers, R G Mensink, M Kenter, et al.
Human Genetics|November 1, 1991
Differential methylation at the 5' and the 3' CCGG sites flanking the X chromosomal hypervariable DXS255 locusR W Hendriks, M E Kraakman, R G Mensink, et al.
Human Molecular Genetics|January 1, 1994
Mutation analysis of the Bruton's tyrosine kinase gene in X-linked agammaglobulinemia: identification of a mutation which affects the same codon as is altered in immunodeficient xid miceM de Weers, R G Mensink, M E Kraakman, et al.
Immunodeficiency|January 1, 1993
X chromosome inactivation patterns in leucocyte populations of female carriers of Wiskott-Aldrich syndrome with an atypical presentationM de Weers, R G Mensink, M E Kraakman, et al.
European Journal of Human Genetics : EJHG|April 11, 2000
SMA carrier testing--validation of hemizygous SMN exon 7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletionH Scheffer, J M Cobben, R G Mensink, et al.
European Journal of Immunology|December 1, 1993
The Bruton's tyrosine kinase gene is expressed throughout B cell differentiation, from early precursor B cell stages preceding immunoglobulin gene rearrangement up to mature B cell stagesM de Weers, M C Verschuren, M E Kraakman, et al.
Clinical and Experimental Immunology|May 1, 1991
Diagnosis of Wiskott-Aldrich syndrome by analysis of the X chromosome inactivation patterns in maternal leucocyte populations using the hypervariable DXS255 locusR W Hendriks, M De Weers, R G Mensink, et al.
Clinical and Experimental Immunology|February 1, 1997
Expression of Bruton's tyrosine kinase in B lymphoblastoid cell lines from X-linked agammaglobulinaemia patientsM De Weers, G M Dingjan, G S Brouns, et al.
Human Pathology|January 11, 2001
Adrenocortical adenocarcinoma in an MSH2 carrier: coincidence or causal relation?M J Berends, A Cats, H Hollema, et al.
Human Genetics|December 1, 1995
Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type IC C Verschuuren-Bemelmans, E R Brunt, M Burton, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|November 1, 1992
Three dinucleotide repeat polymorphisms at the DXS178 locusM de Weers, R G Mensink, M Kenter, et al.
Human Genetics|November 1, 1991
Differential methylation at the 5' and the 3' CCGG sites flanking the X chromosomal hypervariable DXS255 locusR W Hendriks, M E Kraakman, R G Mensink, et al.
Human Molecular Genetics|January 1, 1994
Mutation analysis of the Bruton's tyrosine kinase gene in X-linked agammaglobulinemia: identification of a mutation which affects the same codon as is altered in immunodeficient xid miceM de Weers, R G Mensink, M E Kraakman, et al.
Immunodeficiency|January 1, 1993
X chromosome inactivation patterns in leucocyte populations of female carriers of Wiskott-Aldrich syndrome with an atypical presentationM de Weers, R G Mensink, M E Kraakman, et al.
European Journal of Human Genetics : EJHG|April 11, 2000
SMA carrier testing--validation of hemizygous SMN exon 7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletionH Scheffer, J M Cobben, R G Mensink, et al.
European Journal of Immunology|December 1, 1993
The Bruton's tyrosine kinase gene is expressed throughout B cell differentiation, from early precursor B cell stages preceding immunoglobulin gene rearrangement up to mature B cell stagesM de Weers, M C Verschuren, M E Kraakman, et al.
Clinical and Experimental Immunology|May 1, 1991
Diagnosis of Wiskott-Aldrich syndrome by analysis of the X chromosome inactivation patterns in maternal leucocyte populations using the hypervariable DXS255 locusR W Hendriks, M De Weers, R G Mensink, et al.
Clinical and Experimental Immunology|February 1, 1997
Expression of Bruton's tyrosine kinase in B lymphoblastoid cell lines from X-linked agammaglobulinaemia patientsM De Weers, G M Dingjan, G S Brouns, et al.
Human Pathology|January 11, 2001
Adrenocortical adenocarcinoma in an MSH2 carrier: coincidence or causal relation?M J Berends, A Cats, H Hollema, et al.
Human Genetics|December 1, 1995
Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type IC C Verschuuren-Bemelmans, E R Brunt, M Burton, et al.
Pageof 2