Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development. [electronic resource]
Producer: 20091008Description: 1010-8 p. digitalISSN:- 1476-5438
- Adult
- Animals
- Brain -- embryology
- Chromosomes, Human, Pair 5
- Chromosomes, Human, Pair 8
- Heart -- embryology
- Heart Defects, Congenital -- genetics
- Humans
- Intellectual Disability -- genetics
- Male
- Mice
- Myocardium -- metabolism
- Proto-Oncogene Proteins -- genetics
- RUNX1 Translocation Partner 1 Protein
- Transcription Factors -- genetics
- Translocation, Genetic
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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