researcher · Minna Pöyhönen · YYNN

Minna Pöyhönen

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researcher

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4

Neurofibromatosis type 1 of the child increases birth weight

scientific article published on 24 April 2019

Molecular Analysis of Familial Endometrial Carcinoma: A Manifestation of Hereditary Nonpolyposis Colorectal Cancer or a Separate Syndrome?

Novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathology

scientific article published on 26 March 2014

Chorea-acanthocytosis associated with two novel heterozygous mutations in the VPS13A gene

scientific article published on 31 October 2019

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Websiteresearchportal.helsinki.fi

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