Merel C. Maiburg
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
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Found 8 publications
Analysis of BRCA1, BRCA2 and PALB2 related Fanconi anemia identifies scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes.
Journal: medRxiv : the preprint server for health sciences
Published: June 26, 2025
BRCA1-, BRCA2-, and PALB2-related Fanconi anemia: Scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes.
Journal: American journal of human genetics
Published: May 15, 2025
Lethal neonatal bone marrow failure syndrome with multiple congenital abnormalities, including limb defects, due to a constitutional deletion of 3' MECOM.
Journal: Haematologica
Published: February 14, 2018
Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case-control study.
Journal: BMC research notes
Published: April 08, 2015
Genetic heterogeneity and clinical variability in musculocontractural Ehlers-Danlos syndrome caused by impaired dermatan sulfate biosynthesis.
Journal: Human mutation
Published: November 20, 2014
The genetic origin of Klinefelter syndrome and its effect on spermatogenesis.
Journal: Fertility and sterility
Published: April 02, 2012
Attitudes of Klinefelter men and their relatives towards TESE-ICSI.
Journal: Journal of assisted reproduction and genetics
Published: April 30, 2011
Does the genetic and familial background of males undertaking ICSI affect the outcome?
Journal: Journal of assisted reproduction and genetics
Published: January 08, 2009
Showing 1-8 of 8
Last Updated: 09/26/2026