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Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications
BACKGROUND: The 22q11.2 deletion syndrome is the most frequent genomic disorder with an estimated frequency of 1/4000 live births. The majority of patients (90%) have the same deletion of 3 Mb (Typically Deleted Region, TDR) that results from aberrant recombination at meiosis between region specific...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1855045/ https://ncbi.nlm.nih.gov/pubmed/17397557 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-8-14 |
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