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Person
M.F. Niermeijer
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Publications (44)
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breast
cancer
cell
chromosome
disease
gene
health
lesions
mutations
patients
protein
renal
risk
screening
symptoms
women
Digital Author ID
info:eu-repo/dai/nl/067934250
Publications
(the most recent at the top)
Similar phenotype characteristics comparing familial and sporadic premature ovarian failure.
Mucopolysaccharidosis type IIID: 12 new patients and 15 novel mutations.
Sense of competence in a Dutch sample of informal caregivers of frontotemporal dementia patients.
Frontotemporal dementia: Change of familial caregiver burden and partner relation in a Dutch cohort of 63 patients
A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p.
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