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Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication
BACKGROUND: Interstitial deletions of 3q29 have been recently described as a microdeletion syndrome mediated by nonallelic homologous recombination between low-copy repeats resulting in an ~1.6 Mb common-sized deletion. Given the molecular mechanism causing the deletion, the reciprocal duplication i...
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Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Artigo |
Lenguaje: | Inglês |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2408925/ https://ncbi.nlm.nih.gov/pubmed/18471269 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-1-8 |
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