Maartje C. Van Rij
Nijmegen, GE, Netherlands
Last Updated: 09/26/2026
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Found 12 publications
Comprehensive Recommendations for the Clinical Management of Pregnant Women With Noninvasive Prenatal Test Results Suspicious of a Maternal Malignancy.
Journal: JCO oncology practice
Published: April 12, 2024
All-in-one whole exome sequencing strategy with simultaneous copy number variant, single nucleotide variant and absence-of-heterozygosity analysis in fetuses with structural ultrasound anomalies: A 1-year experience.
Journal: Prenatal diagnosis
Published: October 07, 2022
Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up Study.
Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Published: April 08, 2022
Two novel presentations of KCNMA1-related pathology--Expanding the clinical phenotype of a rare channelopathy.
Journal: Molecular genetics & genomic medicine
Published: November 24, 2020
Correction: Putting genome-wide sequencing in neonates into perspective.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 23, 2018
Putting genome-wide sequencing in neonates into perspective.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: April 17, 2018
Two novel cases expanding the phenotype of SETD2-related overgrowth syndrome.
Journal: American journal of medical genetics. Part A
Published: June 30, 2017
Rothmund-Thomson syndrome and osteoma cutis in a patient previously diagnosed as COPS syndrome.
Journal: European journal of pediatrics
Published: April 01, 2016
The uptake and outcome of prenatal and pre-implantation genetic diagnosis for Huntington's disease in the Netherlands (1998-2008).
Journal: Clinical genetics
Published: December 06, 2012
Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008.
Journal: Clinical genetics
Published: December 06, 2012
Evaluation of exclusion prenatal and exclusion preimplantation genetic diagnosis for Huntington's disease in the Netherlands.
Journal: Clinical genetics
Published: November 10, 2012
Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.
Journal: European journal of human genetics : EJHG
Published: November 11, 2011
Showing 1-12 of 12
Last Updated: 09/26/2026