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DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome.
Wright, J Timothy; Hong, Sung P; Simmons, Darrin; Daly, Bill; Uebelhart, Daniel; Luder, Hans U.
Affiliation
  • Wright JT; Department of Pediatric Dentistry, The University of North, Chapel Hill, North Carolina 27599, USA.Tim_Wright@Dentistry.unc.edu
Am J Med Genet A ; 146A(3): 343-9, 2008 Feb 01.
Article in En | MEDLINE | ID: mdl-18203197
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Transcription Factors / Sequence Deletion / Homeodomain Proteins / Amelogenesis Imperfecta Type of study: Etiology_studies Limits: Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2008 Document type: Article Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Transcription Factors / Sequence Deletion / Homeodomain Proteins / Amelogenesis Imperfecta Type of study: Etiology_studies Limits: Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2008 Document type: Article Country of publication: United States