Morphological analyses and a novel de novo DLX3 mutation associated with tricho-dento-osseous syndrome in a Chinese family.
about
Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta.Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome.Phenotype and genotype analyses in seven families with dentinogenesis imperfecta or dentin dysplasia.A de novo germline mutation of DLX3 in a Brown Swiss calf with tricho-dento-osseus-like syndrome.DLX3-Dependent Regulation of Ion Transporters and Carbonic Anhydrases is Crucial for Enamel Mineralization.
P2860
Morphological analyses and a novel de novo DLX3 mutation associated with tricho-dento-osseous syndrome in a Chinese family.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Morphological analyses and a n ...... syndrome in a Chinese family.
@ast
Morphological analyses and a n ...... syndrome in a Chinese family.
@en
type
label
Morphological analyses and a n ...... syndrome in a Chinese family.
@ast
Morphological analyses and a n ...... syndrome in a Chinese family.
@en
prefLabel
Morphological analyses and a n ...... syndrome in a Chinese family.
@ast
Morphological analyses and a n ...... syndrome in a Chinese family.
@en
P2093
P2860
P356
P1476
Morphological analyses and a n ...... s syndrome in a Chinese family
@en
P2093
P2860
P304
P356
10.1111/EOS.12197
P577
2015-06-24T00:00:00Z