Clinical Utility of Array Comparative Genomic Hybridization: Uncovering Tumor Susceptibility in Individuals with Developmental Delay - 08/08/11
Doi : 10.1016/j.jpeds.2008.07.045
Margaret P. Adam, MD a, ⁎ 
, April N. Justice, MS a, Susan Schelley, MPH b, Andrea Kwan, MS b, Louanne Hudgins, MD b, Christa L. Martin, PhD a
, April N. Justice, MS a, Susan Schelley, MPH b, Andrea Kwan, MS b, Louanne Hudgins, MD b, Christa L. Martin, PhD a a Department of Human Genetics, Emory University School of Medicine, Atlanta, GA
b Department of Pediatrics, Division of Medical Genetics, Stanford University School of Medicine, Stanford, CA
Reprint requests: Dr. Margaret P. Adam, Department of Human Genetics, Emory University School of Medicine, 2165 N. Decatur Road, Decatur, GA 30033Resumen |
Microarray-based comparative genomic hybridization can determine genome-wide copy number alterations at the kilobase level. We highlight the clinical utility of microarray-based comparative genomic hybridization in determining tumor susceptibility in 3 patients with dysmorphic features and developmental delay, likely decreasing both morbidity and mortality in these patients.
El texto completo de este artículo está disponible en PDF.Abbreviations : aCGH, FISH, LFS, PJS
Esquema
| This work was not supported by any grant funds. The authors declare no conflicts of interest. |
© 2009
Mosby, Inc. Reservados todos los derechos.
Vol 154 - N° 1
P. 143-146 - janvier 2009 Regresar al número
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