[HTML][HTML] A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families
MS Chishti, D Muhammad, M Haider… - Journal of human …, 2006 - nature.com
… association with other anomalies, the mode of inheritance is autosomal dominant. … Pakistani
kindreds with an autosomal recessive form of oligodontia with associated dental anomalies. …
kindreds with an autosomal recessive form of oligodontia with associated dental anomalies. …
Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia
K Xuan, F Jin, YL Liu, LT Yuan, LY Wen, FS Yang… - Archives of Oral …, 2008 - Elsevier
… However, reported mutations underlying non-syndromic oligodontia in … family, our
findings are in agreement with previous reports on frequency of tooth loss with MSX1 mutations…
findings are in agreement with previous reports on frequency of tooth loss with MSX1 mutations…
Non-syndromic severe hypodontia caused by a novel frameshift insertion mutation in the homeobox of the MSX1 gene
… the causal gene mutation(s) in a family of two sisters with severe hypodontia (oligodontia) …
well established strategy for discovering rare alleles underlying Mendelian disorders. In this …
well established strategy for discovering rare alleles underlying Mendelian disorders. In this …
[HTML][HTML] Mutations in the MSX1 gene in Turkish children with non-syndromic tooth agenesis and other dental anomalies
D Ceyhan, Z Kirzioglu, NS Calapoglu - Indian journal of dentistry, 2014 - ncbi.nlm.nih.gov
… as a missense mutation, has not been reported in literature. … aiming to determine gene
mutations underlying missing teeth. … anomalies and autosomal recessive form of oligodontia and …
mutations underlying missing teeth. … anomalies and autosomal recessive form of oligodontia and …
[HTML][HTML] Novel MSX1 variants identified in families with nonsyndromic oligodontia
J Zheng, M Yu, H Liu, T Cai, H Feng, Y Liu… - … journal of oral science, 2021 - nature.com
… We found that, among these variants, 75% of the missense … novel MSX1 variants in
Chinese families with oligodontia inherited in an autosomal-dominant manner: three missense …
Chinese families with oligodontia inherited in an autosomal-dominant manner: three missense …
[HTML][HTML] Next generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontia
O Bonczek, P Bielik, P Krejčí, T Zeman… - PLoS …, 2018 - journals.plos.org
… Signals from the underlying signalling centres are mediated by … one case of autosomal
recessive oligodontia has appeared [… in Japanese family with non-syndromic oligodontia. They …
recessive oligodontia has appeared [… in Japanese family with non-syndromic oligodontia. They …
[HTML][HTML] Genetic Anomalies and Tooth Agenesis
M Shahid - Biomedical and Pharmacology Journal, 2015 - biomedpharmajournal.org
… To the best of our knowledge, many mutations have been detected in the MSX1 gene, most
… Another missense mutation was detected in the Pakistani families affected with oligodontia. …
… Another missense mutation was detected in the Pakistani families affected with oligodontia. …
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
… agenesis are missense or nonsense mutations. … Therefore, we conclude that this non-stop
mutation in MSX1 causes autosomal dominant non-syndromic oligodontia in our study family. …
mutation in MSX1 causes autosomal dominant non-syndromic oligodontia in our study family. …
[PDF][PDF] Role of MSX1 Gene in Tooth Agensis and Non-Syndromic Cleft/Lip Palate: A Literature Review
MDS Sneha Singh, TP Chaturvedi, AV Parihar… - IJO, 2019 - researchgate.net
… form of oligodontia with associated dental anomalies. Locus in this … tooth agenesis and
detected a novel nonsense mutation (c.416G>A) in exon 1 of Msx1 from a family with oligodontia. …
detected a novel nonsense mutation (c.416G>A) in exon 1 of Msx1 from a family with oligodontia. …
A novel MSX1 intronic mutation associated with autosomal dominant non-syndromic oligodontia in a large Chinese family pedigree
J Xue, Q Gao, Y Huang, X Zhang, P Yang, DS Cram… - Clinica Chimica …, 2016 - Elsevier
… Tooth agenesis is a highly heterogeneous genetic disorder which can show an autosomal
recessive, autosomal dominant or X-linked … of MSX1 mutations, the underlying mechanisms …
recessive, autosomal dominant or X-linked … of MSX1 mutations, the underlying mechanisms …