Table of Contents
Tiivistelmä. - Abstract.
Kyttälä, Mira
- University of Helsinki
2006
9517406118
951740610X
Abnormalities, Multiple Chromosomes, Human, Pair 17 Encephalocele Genetic Diseases, Inborn Genome, Human Meningocele Mutation Polycystic Kidney, Autosomal Recessive Polydactyly Proteome epämuodostumat geenivirheet kehityshäiriöt Meckelin oireyhtymä perinnölliset taudit missbildningar gendefekter utvecklingsstörningar Meckels syndrom ärftliga sjukdomar Academic Dissertations väitöskirjat e-böcker doktorsavhandlingar
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