R J Sinke - JoVE Visualize

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Cancer Genetics and Cytogenetics|October 15, 1993

Overrepresentation of chromosome 12p sequences and karyotypic evolution in i(12p)-negative testicular germ-cell tumors revealed by fluorescence in situ hybridizationR F Suijkerbuijk, R J Sinke, A M Meloni, et al.

Cancer Genetics and Cytogenetics|July 15, 1997

Fine mapping of the human renal oncocytoma-associated translocation (5;11)(q35;q13) breakpointR J Sinke, T Dijkhuizen, B Janssen, et al.

Archives of Neurology|November 16, 2001

Clinical and molecular correlations in spinocerebellar ataxia type 6: a study of 24 Dutch familiesR J Sinke, E F Ippel, C M Diepstraten, et al.

Cancer Genetics and Cytogenetics|December 1, 1993

Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2R F Suijkerbuijk, A M Meloni, R J Sinke, et al.

Neurology|December 25, 2003

Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia familyB P C van de Warrenburg, D S Verbeek, S J Piersma, et al.

Molecular Psychiatry|April 28, 2001

Association between an agouti-related protein gene polymorphism and anorexia nervosaT Vink, A Hinney, A A van Elburg, et al.

American Journal of Human Genetics|April 8, 2003

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15qS C Bakker, E M van der Meulen, J K Buitelaar, et al.

Prenatal Diagnosis|October 19, 2005

Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA)R Hochstenbach, J Meijer, J van de Brug, et al.

Neurology|March 13, 2002

Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysisB P C van de Warrenburg, R J Sinke, C C Verschuuren-Bemelmans, et al.

Scientific Reports|May 14, 2017

Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal TestingL F Johansson, E N de Boer, H A de Weerd, et al.

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Showing results (31-40 of 43) with videos related to

Sort By:

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Cancer Genetics and Cytogenetics|October 15, 1993

Overrepresentation of chromosome 12p sequences and karyotypic evolution in i(12p)-negative testicular germ-cell tumors revealed by fluorescence in situ hybridizationR F Suijkerbuijk, R J Sinke, A M Meloni, et al.

Cancer Genetics and Cytogenetics|July 15, 1997

Fine mapping of the human renal oncocytoma-associated translocation (5;11)(q35;q13) breakpointR J Sinke, T Dijkhuizen, B Janssen, et al.

Archives of Neurology|November 16, 2001

Clinical and molecular correlations in spinocerebellar ataxia type 6: a study of 24 Dutch familiesR J Sinke, E F Ippel, C M Diepstraten, et al.

Cancer Genetics and Cytogenetics|December 1, 1993

Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2R F Suijkerbuijk, A M Meloni, R J Sinke, et al.

Neurology|December 25, 2003

Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia familyB P C van de Warrenburg, D S Verbeek, S J Piersma, et al.

Molecular Psychiatry|April 28, 2001

Association between an agouti-related protein gene polymorphism and anorexia nervosaT Vink, A Hinney, A A van Elburg, et al.

American Journal of Human Genetics|April 8, 2003

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15qS C Bakker, E M van der Meulen, J K Buitelaar, et al.

Prenatal Diagnosis|October 19, 2005

Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA)R Hochstenbach, J Meijer, J van de Brug, et al.

Neurology|March 13, 2002

Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysisB P C van de Warrenburg, R J Sinke, C C Verschuuren-Bemelmans, et al.

Scientific Reports|May 14, 2017

Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal TestingL F Johansson, E N de Boer, H A de Weerd, et al.

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