Found: 3
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De novo t(12;17)(p13.3;q21.3) translocation with a breakpoint near the 5′ end of the HOXB gene cluster in a patient with developmental delay and skeletal malformations.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 5, p. 570, doi. 10.1038/sj.ejhg.5201795
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- Publication type:
- Article
A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.
- Published in:
- 2003
- By:
- Publication type:
- journal article
New cytogenetically visible copy number variant in region 8q21.2.
- Published in:
- Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 1, doi. 10.1186/1755-8166-4-1
- By:
- Publication type:
- Article