BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1

BACKGROUND: Microdeletion of the chromosome 22q11.2 region is the most common genetic aberration among patients with velocardiofacial syndrome (VCFS) but a subset of subjects do not show alterations of this chromosome region. METHODS: We analyzed 18 patients with VCFS-like features by comparative ge...

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Detalles Bibliográficos
Autores principales: Brunet, Anna, Armengol, Lluís, Heine, Damià, Rosell, Jordi, García-Aragonés, Manel, Gabau, Elisabeth, Estivill, Xavier, Guitart, Miriam
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Research article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805625/
https://www.ncbi.nlm.nih.gov/pubmed/20030804
http://dx.doi.org/10.1186/1471-2350-10-144

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805625/
https://www.ncbi.nlm.nih.gov/pubmed/20030804
http://dx.doi.org/10.1186/1471-2350-10-144

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