A novel c.581C>T transition localized in a highly conserved homeobox sequence ofMSX1: is it responsible for oligodontia?

No abstract is available for this paper.

• Publication year

  2010

• Venue

  Journal of Applied Genetics

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/BF03194616PMID 16682758
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• for Vietnamese

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• Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer.

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• MSX1, PAX9, and TGFA Contribute to Tooth Agenesis in Humans

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• Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia.

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• Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

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• Novel missense mutations and a 288‐bp exonic insertion in PAX9 in families with autosomal dominant hypodontia

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• Oligodontia Management in a Resource-Limited Setting: Two Case Reports and Review of Literature

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• An Aberrant Splice Acceptor Site Due to a Novel Intronic Nucleotide Substitution in MSX1 Gene Is the Cause of Congenital Tooth Agenesis in a Japanese Family

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• Tooth agenesis patterns and phenotype variation in a cohort of Belgian patients with hypodontia and oligodontia clustered in 79 families with their pedigrees.

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• ASSOCIATION BETWEEN POLYMORPHISM IN THE PROMOTER REGION (G/C-915) OF PAX9 GENE AND THIRD MOLAR AGENESIS

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