DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
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1. Developmental expression of the homeobox protein Distal-less 3 and its relationship to progesterone production in mouse placenta
2. Amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome: separate conditions or a spectrum of disease?
3. DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism
4. Increased bone density associated with DLX3 mutation in the tricho-dento-osseous syndrome
5. Dental abnormalities in the tricho-dento-osseous syndrome
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