A New Chromosome X Exon-Specific Microarray Platform for Screening of Patients with X-Linked Disorders

Recent studies and advances in high-density oligonucleotide arrays have shown that microdeletions and microduplications occur at a high frequency in the human genome, causing various genetic conditions including mental retardation. Thus far little is known about the pathways leading to this disease,...

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Detalhes bibliográficos
Main Authors: Bashiardes, Stavros, Kousoulidou, Ludmila, van Bokhoven, Hans, Ropers, Hans-Hilger, Chelly, Jamel, Moraine, Claude, de Brouwer, Arjan P.M., Van Esch, Hilde, Froyen, Guy, Patsalis, Philippos C.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2009
Assuntos:
Regular Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2765755/
https://ncbi.nlm.nih.gov/pubmed/19779134
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/jmoldx.2009.090086
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