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Showing results (41-50 of 52) with videos related to

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Human Reproduction (Oxford, England)|July 15, 2016
Klinefelter syndrome and fertility: sperm preservation should not be offered to children with Klinefelter syndromeS Franik, Y Hoeijmakers, K D'Hauwers, et al.
Human Mutation|February 5, 1998
Identification of ATM mutations using extended RT-PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A-T mutations in IsraelS Gilad, R Khosravi, R Harnik, et al.
Neurology|September 6, 2007
Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHDJ C de Greef, M Wohlgemuth, O A Chan, et al.
Kidney International|February 14, 1998
A familial case of renal cell carcinoma and a t(2;3) chromosome translocationM I Koolen, A P van der Meyden, D Bodmer, et al.
Nature Genetics|June 10, 1998
Positional cloning of the gene for Nijmegen breakage syndromeS Matsuura, H Tauchi, A Nakamura, et al.
American Journal of Medical Genetics. Part A|August 21, 2007
ICF syndrome: high variability of the chromosomal phenotype and association with classical Hodgkin lymphomaC Schuetz, G Barbi, T F E Barth, et al.
Genes, Chromosomes & Cancer|April 3, 2001
Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15)M J Eleveld, D Bodmer, G Merkx, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 4, 2014
Plasma circulating tumor DNA as an alternative to metastatic biopsies for mutational analysis in breast cancerF Rothé, J-F Laes, D Lambrechts, et al.
American Journal of Human Genetics|June 23, 1998
Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotypeK M Cerosaletti, E Lange, H M Stringham, et al.
Human Molecular Genetics|December 14, 2001
DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genesM Ehrlich, K L Buchanan, F Tsien, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Human Reproduction (Oxford, England)|July 15, 2016
Klinefelter syndrome and fertility: sperm preservation should not be offered to children with Klinefelter syndromeS Franik, Y Hoeijmakers, K D'Hauwers, et al.
Human Mutation|February 5, 1998
Identification of ATM mutations using extended RT-PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A-T mutations in IsraelS Gilad, R Khosravi, R Harnik, et al.
Neurology|September 6, 2007
Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHDJ C de Greef, M Wohlgemuth, O A Chan, et al.
Kidney International|February 14, 1998
A familial case of renal cell carcinoma and a t(2;3) chromosome translocationM I Koolen, A P van der Meyden, D Bodmer, et al.
Nature Genetics|June 10, 1998
Positional cloning of the gene for Nijmegen breakage syndromeS Matsuura, H Tauchi, A Nakamura, et al.
American Journal of Medical Genetics. Part A|August 21, 2007
ICF syndrome: high variability of the chromosomal phenotype and association with classical Hodgkin lymphomaC Schuetz, G Barbi, T F E Barth, et al.
Genes, Chromosomes & Cancer|April 3, 2001
Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15)M J Eleveld, D Bodmer, G Merkx, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 4, 2014
Plasma circulating tumor DNA as an alternative to metastatic biopsies for mutational analysis in breast cancerF Rothé, J-F Laes, D Lambrechts, et al.
American Journal of Human Genetics|June 23, 1998
Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotypeK M Cerosaletti, E Lange, H M Stringham, et al.
Human Molecular Genetics|December 14, 2001
DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genesM Ehrlich, K L Buchanan, F Tsien, et al.
Pageof 6