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Title: A novel MSX1 mutation in hypodontia
Authors: De Muynck, Stijn ×
Schollen, E
Matthijs, Gert
Verdonck, Anna
Devriendt, Koenraad
Carels, Carine #
Issue Date: Aug-2004
Series Title: American Journal of Medical Genetics A vol:128A issue:4 pages:401-3
Abstract: MSX1 mutations have been reported in four unrelated families with autosomal dominant tooth agenesis. In one family, some individuals also had cleft lip and/or palate. We have identified a novel MSX1 mutation (559 C --> T, resulting in Gln187Stop) in three individuals of one family.
ISSN: 1552-4825
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Clinical Genetics Section (-)
Clinical Residents Dentistry
Interdisciplinary Research Facility Life Sciences, Campus Kulak Kortrijk
Department of Human Genetics - miscellaneous
Faculty of Medicine - miscellaneous
× corresponding author
# (joint) last author

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