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M M Mannens

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

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Cancer Genetics and Cytogenetics|July 15, 1992
Cytogenetics and molecular genetics of Wilms' tumor of childhoodR M Slater, M M Mannens
Nederlands Tijdschrift Voor Geneeskunde|April 19, 1997
[Iatrogenic collapse; can this be prevented?]A A Wilde, M M Mannens
Nederlands Tijdschrift Voor Geneeskunde|July 6, 2000
[Decoding of the human genome: a milestone, but not the end of the road]N J Leschot, M M Mannens
Lancet (London, England)|May 16, 1992
Imprinting and Beckwith-Wiedemann syndromeJ M Hoovers, A J Dietrich, M M Mannens
Human Genetics|September 1, 1992
The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumorA M van den Ouweland, M Verdijk, M M Mannens, et al.
Human Mutation|June 30, 2000
A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: determination of the molecular basisC M Aalfs, G B Salieb-Beugelaar, R J Wanders, et al.
Human Molecular Genetics|February 22, 2001
Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWSJ Bliek, S M Maas, J M Ruijter, et al.
Journal of Medical Genetics|December 1, 1995
Further delineation of the partial proximal trisomy 10q syndromeC M Aalfs, J M Hoovers, M A Nieste-Otter, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studiesR van den Bogaard, C A Fijen, M G Schipper, et al.
Human Genetics|August 15, 2000
Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3A V Postma, C R Bezzina, J F de Vries, et al.
Pageof 3

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

Sort By:
Pageof 3
Cancer Genetics and Cytogenetics|July 15, 1992
Cytogenetics and molecular genetics of Wilms' tumor of childhoodR M Slater, M M Mannens
Nederlands Tijdschrift Voor Geneeskunde|April 19, 1997
[Iatrogenic collapse; can this be prevented?]A A Wilde, M M Mannens
Nederlands Tijdschrift Voor Geneeskunde|July 6, 2000
[Decoding of the human genome: a milestone, but not the end of the road]N J Leschot, M M Mannens
Lancet (London, England)|May 16, 1992
Imprinting and Beckwith-Wiedemann syndromeJ M Hoovers, A J Dietrich, M M Mannens
Human Genetics|September 1, 1992
The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumorA M van den Ouweland, M Verdijk, M M Mannens, et al.
Human Mutation|June 30, 2000
A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: determination of the molecular basisC M Aalfs, G B Salieb-Beugelaar, R J Wanders, et al.
Human Molecular Genetics|February 22, 2001
Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWSJ Bliek, S M Maas, J M Ruijter, et al.
Journal of Medical Genetics|December 1, 1995
Further delineation of the partial proximal trisomy 10q syndromeC M Aalfs, J M Hoovers, M A Nieste-Otter, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studiesR van den Bogaard, C A Fijen, M G Schipper, et al.
Human Genetics|August 15, 2000
Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3A V Postma, C R Bezzina, J F de Vries, et al.
Pageof 3