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Molekulární aspekty hypodoncie
Fleischmannová, Jana ; Krejčí, P. ; Matalová, Eva ; Míšek, Ivan
Numeric dental anomalies are the most common craniofacial congenital malformations in humans. More than 20 % of human population miss one or more third molars, approximately 5 % of population display agenesis of another tooth. In this contribution molecular events underlying tooth formation (more than 200 genes have been identified so far) and defects in tooth germ formation are correlated. Both syndromic forms of hypodonia (e.g. Rieger syndrome, anhidrotic ectodermal dysplasia) and non-syndromic forms (related to pax9, msx1, axin2) were investigated.

National Repository of Grey Literature : 13 records found   previous11 - 13  jump to record:
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2 Míšek, I.
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