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Marjolijn C J Jongmans

Showing results (1-10 of 53) with videos related to

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Cancer Letters|June 25, 2017
Immunotherapy holds the key to cancer treatment and prevention in constitutional mismatch repair deficiency (CMMRD) syndromeHarm Westdorp, Sigrid Kolders, Nicoline Hoogerbrugge, et al.
Familial Cancer|June 25, 2021
Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working GroupJette J Bakhuizen, Helen Hanson, Karin van der Tuin, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|August 11, 2018
Severe Positional Central Sleep Apnea in an Asymptomatic Adult With a <i>PHOX2B</i> Frameshift MutationHennie C J P Janssen, Anneke T Vulto-van Silfhout, Marjolijn C J Jongmans, et al.
Pediatric Blood & Cancer|September 12, 2022
The pathophysiology of bilateral and multifocal Wilms tumors: What we can learn from the study of predisposition syndromesNils Welter, Jack Brzezinski, Amy Treece, et al.
European Journal of Human Genetics : EJHG|June 16, 2018
Cancer prevention by aspirin in children with Constitutional Mismatch Repair Deficiency (CMMRD)Erika K S M Leenders, Harm Westdorp, Roger J Brüggemann, et al.
European Journal of Medical Genetics|January 31, 2016
Recognition of genetic predisposition in pediatric cancer patients: An easy-to-use selection toolMarjolijn C J Jongmans, Jan L C M Loeffen, Esmé Waanders, et al.
European Journal of Medical Genetics|May 13, 2008
Exon copy number alterations of the CHD7 gene are not a major cause of CHARGE and CHARGE-like syndromeJorieke E H Bergman, Ilse de Wijs, Marjolijn C J Jongmans, et al.
European Journal of Human Genetics : EJHG|February 27, 2024
Experiences of pediatric cancer patients (age 12-18 years) with extensive germline sequencing for cancer predisposition: a qualitative studySebastian B B Bon, Roel H P Wouters, Jette J Bakhuizen, et al.
Psycho-Oncology|August 13, 2022
Parents' experiences with large-scale sequencing for genetic predisposition in pediatric renal cancer: A qualitative studySebastian B B Bon, Roel H P Wouters, Janna A Hol, 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.
Pageof 6

Showing results (1-10 of 53) with videos related to

Sort By:
Pageof 6
Cancer Letters|June 25, 2017
Immunotherapy holds the key to cancer treatment and prevention in constitutional mismatch repair deficiency (CMMRD) syndromeHarm Westdorp, Sigrid Kolders, Nicoline Hoogerbrugge, et al.
Familial Cancer|June 25, 2021
Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working GroupJette J Bakhuizen, Helen Hanson, Karin van der Tuin, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|August 11, 2018
Severe Positional Central Sleep Apnea in an Asymptomatic Adult With a <i>PHOX2B</i> Frameshift MutationHennie C J P Janssen, Anneke T Vulto-van Silfhout, Marjolijn C J Jongmans, et al.
Pediatric Blood & Cancer|September 12, 2022
The pathophysiology of bilateral and multifocal Wilms tumors: What we can learn from the study of predisposition syndromesNils Welter, Jack Brzezinski, Amy Treece, et al.
European Journal of Human Genetics : EJHG|June 16, 2018
Cancer prevention by aspirin in children with Constitutional Mismatch Repair Deficiency (CMMRD)Erika K S M Leenders, Harm Westdorp, Roger J Brüggemann, et al.
European Journal of Medical Genetics|January 31, 2016
Recognition of genetic predisposition in pediatric cancer patients: An easy-to-use selection toolMarjolijn C J Jongmans, Jan L C M Loeffen, Esmé Waanders, et al.
European Journal of Medical Genetics|May 13, 2008
Exon copy number alterations of the CHD7 gene are not a major cause of CHARGE and CHARGE-like syndromeJorieke E H Bergman, Ilse de Wijs, Marjolijn C J Jongmans, et al.
European Journal of Human Genetics : EJHG|February 27, 2024
Experiences of pediatric cancer patients (age 12-18 years) with extensive germline sequencing for cancer predisposition: a qualitative studySebastian B B Bon, Roel H P Wouters, Jette J Bakhuizen, et al.
Psycho-Oncology|August 13, 2022
Parents' experiences with large-scale sequencing for genetic predisposition in pediatric renal cancer: A qualitative studySebastian B B Bon, Roel H P Wouters, Janna A Hol, 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.
Pageof 6