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Illja J Diets

Showing results (1-10 of 14) with videos related to

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Haematologica|September 15, 2018
Somatic reversion events point towards Marjolijn C J Jongmans, Illja J Diets, Paola Quarello, et al.
The Journal of Pathology|February 10, 2021
TRIM28 variants and Wilms' tumour predispositionJanna A Hol, Illja J Diets, Ronald R de Krijger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2018
A recurrent de novo missense pathogenic variant in SMARCB1 causes severe intellectual disability and choroid plexus hyperplasia with resultant hydrocephalusIllja J Diets, Trine Prescott, Neena L Champaigne, et al.
Familial Cancer|June 1, 2021
Selection criteria for assembling a pediatric cancer predisposition syndrome gene panelAnna Byrjalsen, Illja J Diets, Jette Bakhuizen, et al.
Leukemia & Lymphoma|December 24, 2015
Clinical features of patients with nodal marginal zone lymphoma compared to follicular lymphoma: similar presentation, but differences in prognostic factors and rate of transformationMichiel van den Brand, Walter J F M van der Velden, Illja J Diets, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|June 26, 2020
Clinical, Pathology, Genetic, and Molecular Features of Colorectal Tumors in Adolescents and Adults 25 Years or YoungerRicharda M de Voer, Illja J Diets, Rachel S van der Post, et al.
International Journal of Cancer|January 30, 2019
TRIM28 haploinsufficiency predisposes to Wilms tumorIllja J Diets, Juliane Hoyer, Arif B Ekici, et al.
Life Science Alliance|January 5, 2024
<i>USP27X</i> variants underlying X-linked intellectual disability disrupt protein function via distinct mechanismsIntisar Koch, Maya Slovik, Yuling Zhang, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 21, 2018
High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with CancerIllja J Diets, Esmé Waanders, Marjolijn J Ligtenberg, et al.
Nucleic Acids Research|December 5, 2019
Ribosomal protein gene RPL9 variants can differentially impair ribosome function and cellular metabolismMarco Lezzerini, Marianna Penzo, Marie-Françoise O'Donohue, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Haematologica|September 15, 2018
Somatic reversion events point towards Marjolijn C J Jongmans, Illja J Diets, Paola Quarello, et al.
The Journal of Pathology|February 10, 2021
TRIM28 variants and Wilms' tumour predispositionJanna A Hol, Illja J Diets, Ronald R de Krijger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2018
A recurrent de novo missense pathogenic variant in SMARCB1 causes severe intellectual disability and choroid plexus hyperplasia with resultant hydrocephalusIllja J Diets, Trine Prescott, Neena L Champaigne, et al.
Familial Cancer|June 1, 2021
Selection criteria for assembling a pediatric cancer predisposition syndrome gene panelAnna Byrjalsen, Illja J Diets, Jette Bakhuizen, et al.
Leukemia & Lymphoma|December 24, 2015
Clinical features of patients with nodal marginal zone lymphoma compared to follicular lymphoma: similar presentation, but differences in prognostic factors and rate of transformationMichiel van den Brand, Walter J F M van der Velden, Illja J Diets, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|June 26, 2020
Clinical, Pathology, Genetic, and Molecular Features of Colorectal Tumors in Adolescents and Adults 25 Years or YoungerRicharda M de Voer, Illja J Diets, Rachel S van der Post, et al.
International Journal of Cancer|January 30, 2019
TRIM28 haploinsufficiency predisposes to Wilms tumorIllja J Diets, Juliane Hoyer, Arif B Ekici, et al.
Life Science Alliance|January 5, 2024
<i>USP27X</i> variants underlying X-linked intellectual disability disrupt protein function via distinct mechanismsIntisar Koch, Maya Slovik, Yuling Zhang, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 21, 2018
High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with CancerIllja J Diets, Esmé Waanders, Marjolijn J Ligtenberg, et al.
Nucleic Acids Research|December 5, 2019
Ribosomal protein gene RPL9 variants can differentially impair ribosome function and cellular metabolismMarco Lezzerini, Marianna Penzo, Marie-Françoise O'Donohue, et al.
Pageof 2