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
Background Tooth agenesis is a common developmental dental anomaly. The aim of the
study was to identify the causal genetic mutation in a four-generation Chinese family …
被引用次数：9 相关文章

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… - Clinica Chimica Acta; …, 2016 - europepmc.org
Background Tooth agenesis is a common developmental dental anomaly. The aim of the
study was to identify the causal genetic mutation in a four-generation Chinese family …

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… - … journal of clinical …, 2016 - pubmed.ncbi.nlm.nih.gov
Background Tooth agenesis is a common developmental dental anomaly. The aim of the
study was to identify the causal genetic mutation in a four-generation Chinese family …

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 - infona.pl
Tooth agenesis is a common developmental dental anomaly. The aim of the study was to
identify the causal genetic mutation in a four-generation Chinese family affected with non …