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Characterization of the TBX5 binding site and analysis of mutations that cause Holt-Oram syndrome.
Ghosh, T K; Packham, E A; Bonser, A J; Robinson, T E; Cross, S J; Brook, J D.
Affiliation
  • Ghosh TK; Institute of Genetics, University of Nottingham, Queen's Medical Centre, Nottingham NG7 2UH, UK.
Hum Mol Genet ; 10(18): 1983-94, 2001 Sep 01.
Article in En | MEDLINE | ID: mdl-11555635
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Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Limb Deformities, Congenital / T-Box Domain Proteins / Fetal Proteins / Heart Defects, Congenital Type of study: Prognostic_studies Limits: Animals Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2001 Document type: Article Affiliation country: Reino Unido Country of publication: Reino Unido
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Limb Deformities, Congenital / T-Box Domain Proteins / Fetal Proteins / Heart Defects, Congenital Type of study: Prognostic_studies Limits: Animals Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2001 Document type: Article Affiliation country: Reino Unido Country of publication: Reino Unido