Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications
<p>Abstract</p> <p>Background</p> <p>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 meiosi...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BMC
2007-04-01
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| Serie: | BMC Medical Genetics |
| Accesso online: | http://www.biomedcentral.com/1471-2350/8/14 |
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