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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 predisposition
Janna 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 hydrocephalus
Illja J Diets, Trine Prescott, Neena L Champaigne, et al.
Familial Cancer
|
June 1, 2021
Selection criteria for assembling a pediatric cancer predisposition syndrome gene panel
Anna 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 transformation
Michiel 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 Younger
Richarda 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 tumor
Illja 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 mechanisms
Intisar 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 Cancer
Illja 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 metabolism
Marco Lezzerini, Marianna Penzo, Marie-Françoise O'Donohue, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 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 predisposition
Janna 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 hydrocephalus
Illja J Diets, Trine Prescott, Neena L Champaigne, et al.
Familial Cancer
|
June 1, 2021
Selection criteria for assembling a pediatric cancer predisposition syndrome gene panel
Anna 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 transformation
Michiel 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 Younger
Richarda 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 tumor
Illja 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 mechanisms
Intisar 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 Cancer
Illja 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 metabolism
Marco Lezzerini, Marianna Penzo, Marie-Françoise O'Donohue, et al.
Page
of 2