A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia
SW Wong, HC Liu, D Han, HG Chang, HS Zhao… - …, 2014 - academic.oup.com
Oligodontia, which is the congenital absence of six or more permanent teeth, excluding the
third molars, may contribute to masticatory dysfunction, speech alteration, aesthetic …
third molars, may contribute to masticatory dysfunction, speech alteration, aesthetic …
[PDF][PDF] A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia
SW Wong, HC Liu, D Han, HG Chang, HS Zhao… - 2014 - researchgate.net
MSX1 in a Chinese family with autosomal dominant non-syndromic oligodontia. This novel
mutation substitutes the stop codon with a tyrosine residue, potentially adding 48 amino …
mutation substitutes the stop codon with a tyrosine residue, potentially adding 48 amino …
A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia
SW Wong, HC Liu, D Han, HG Chang, HS Zhao… - Mutagenesis, 2014 - ss.bjmu.edu.cn
MSX1 in a Chinese family with autosomal dominant non-syndromic oligodontia. This novel
mutation substitutes the stop codon with a tyrosine residue, potentially adding 48 amino …
mutation substitutes the stop codon with a tyrosine residue, potentially adding 48 amino …
A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia.
SW Wong, HC Liu, D Han, HG Chang, HS Zhao… - …, 2014 - search.ebscohost.com
Oligodontia, which is the congenital absence of six or more permanent teeth, excluding the
third molars, may contribute to masticatory dysfunction, speech alteration, aesthetic …
third molars, may contribute to masticatory dysfunction, speech alteration, aesthetic …
[引用][C] A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia
SW Wong, HC Liu, D Han, HG Chang, HS Zhao… - Mutagenesis, 2014 - cir.nii.ac.jp
[引用][C] A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia
SW Wong, HC Liu, D Han, HG Chang, HS Zhao… - Mutagenesis, 2014 - rekq.net
MSX1 in a Chinese family with autosomal dominant non-syndromic oligodontia. This novel
mutation substitutes the stop codon with a tyrosine residue, potentially adding 48 amino …
mutation substitutes the stop codon with a tyrosine residue, potentially adding 48 amino …
A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia.
SW Wong, HC Liu, D Han, HG Chang, HS Zhao… - Mutagenesis, 2014 - europepmc.org
Oligodontia, which is the congenital absence of six or more permanent teeth, excluding the
third molars, may contribute to masticatory dysfunction, speech alteration, aesthetic …
third molars, may contribute to masticatory dysfunction, speech alteration, aesthetic …
A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia
SW Wong, HC Liu, D Han, HG Chang… - …, 2014 - pubmed.ncbi.nlm.nih.gov
Oligodontia, which is the congenital absence of six or more permanent teeth, excluding the
third molars, may contribute to masticatory dysfunction, speech alteration, aesthetic …
third molars, may contribute to masticatory dysfunction, speech alteration, aesthetic …
[PDF][PDF] A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia
SW Wong, HC Liu, D Han, HG Chang, HS Zhao… - 2014 - Citeseer
MSX1 in a Chinese family with autosomal dominant non-syndromic oligodontia. This novel
mutation substitutes the stop codon with a tyrosine residue, potentially adding 48 amino …
mutation substitutes the stop codon with a tyrosine residue, potentially adding 48 amino …
[PDF][PDF] A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia
SW Wong, HC Liu, D Han, HG Chang, HS Zhao… - Mutagenesis, 2014 - Citeseer
MSX1 in a Chinese family with autosomal dominant non-syndromic oligodontia. This novel
mutation substitutes the stop codon with a tyrosine residue, potentially adding 48 amino …
mutation substitutes the stop codon with a tyrosine residue, potentially adding 48 amino …