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D Smeets

Showing results (31-40 of 52) with videos related to

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Journal of Medical Genetics|January 1, 1997
At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocationD Smeets, C van Ravenswaaij, J de Pater, et al.
Human Molecular Genetics|August 1, 1993
No imprinting involved in the expression of DM-kinase mRNAs in mouse and human tissuesG Jansen, M Bartolomei, V Kalscheuer, et al.
The European Respiratory Journal|May 31, 2011
The TERT-CLPTM1L locus for lung cancer predisposes to bronchial obstruction and emphysemaE Wauters, D Smeets, J Coolen, et al.
Journal of Intellectual Disability Research : JIDR|March 8, 2011
Changes in yearly birth prevalence rates of children with Down syndrome in the period 1986-2007 in The NetherlandsG de Graaf, M Haveman, R Hochstenbach, et al.
Andrologia|March 8, 2018
Klinefelter syndrome and fertility-Impact of X-chromosomal inheritance on spermatogenesisS Franik, D Smeets, G van de Zande, et al.
International Journal of Molecular Medicine|December 17, 2008
Protein profiling of non-malignant and malignant ascites by SELDI-TOF MS: proof of principleT Braunschweig, R C Krieg, R Bar-Or, et al.
Reproduction, Fertility, and Development|February 16, 2016
Detection of cross-sex chimerism in the common marmoset monkey (Callithrix jacchus) in interphase cells using fluorescence in situ hybridisation probes specific for the marmoset X and Y chromosomesE Wedi, S Müller, M Neusser, et al.
American Journal of Medical Genetics|February 1, 1991
Multipoint linkage analysis of DXS369 and DXS304 in fragile X familiesB A van Oost, A Smits, J C Dreesen, et al.
American Journal of Human Genetics|June 1, 1997
Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24S Matsuura, C Weemaes, D Smeets, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|November 23, 2013
The rs1800716 variant in CYP2D6 is associated with an increased double endometrial thickness in postmenopausal women on tamoxifenA-S Dieudonné, D Lambrechts, D Smeets, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|January 1, 1997
At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocationD Smeets, C van Ravenswaaij, J de Pater, et al.
Human Molecular Genetics|August 1, 1993
No imprinting involved in the expression of DM-kinase mRNAs in mouse and human tissuesG Jansen, M Bartolomei, V Kalscheuer, et al.
The European Respiratory Journal|May 31, 2011
The TERT-CLPTM1L locus for lung cancer predisposes to bronchial obstruction and emphysemaE Wauters, D Smeets, J Coolen, et al.
Journal of Intellectual Disability Research : JIDR|March 8, 2011
Changes in yearly birth prevalence rates of children with Down syndrome in the period 1986-2007 in The NetherlandsG de Graaf, M Haveman, R Hochstenbach, et al.
Andrologia|March 8, 2018
Klinefelter syndrome and fertility-Impact of X-chromosomal inheritance on spermatogenesisS Franik, D Smeets, G van de Zande, et al.
International Journal of Molecular Medicine|December 17, 2008
Protein profiling of non-malignant and malignant ascites by SELDI-TOF MS: proof of principleT Braunschweig, R C Krieg, R Bar-Or, et al.
Reproduction, Fertility, and Development|February 16, 2016
Detection of cross-sex chimerism in the common marmoset monkey (Callithrix jacchus) in interphase cells using fluorescence in situ hybridisation probes specific for the marmoset X and Y chromosomesE Wedi, S Müller, M Neusser, et al.
American Journal of Medical Genetics|February 1, 1991
Multipoint linkage analysis of DXS369 and DXS304 in fragile X familiesB A van Oost, A Smits, J C Dreesen, et al.
American Journal of Human Genetics|June 1, 1997
Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24S Matsuura, C Weemaes, D Smeets, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|November 23, 2013
The rs1800716 variant in CYP2D6 is associated with an increased double endometrial thickness in postmenopausal women on tamoxifenA-S Dieudonné, D Lambrechts, D Smeets, et al.
Pageof 6