Prenatal diagnosis using array CGH

Methods in Molecular Biology

Volumn 444, Issue , 2008, Pages 59-69

  Kashork, Catherine D ^a   Theisen, Aaron ^a   Shaffer, Lisa G ^a,b  

^a Signature Genomic Laboratories LLC   (United States)

^b WASHINGTON STATE UNIVERSITY   (United States)

Author keywords

Array CGH; Comparative genomic hybridization; Congenital malformations; Microarray; Prenatal diagnosis

Indexed keywords

EID: 84934444045     PISSN: 10643745     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-59745-66-9_5     Document Type: Article

References (3)

1. Barch, M. J., Knutsen, T., and Spurbeck, J. L. (eds.) (1997) The AGT cytogenetics laboratory manual. Lippincott Williams & Wilkins, Philadelphia, PA.
2. Hui, A. B., Lo, K. W., Yin, X. L., Poon, W. S., and Ng, H. K. (2001) Detection of multiple gene amplifications in glioblastoma multiforme using array-based comparative genomic hybridization. Lab. Invest. 81, 717-723.
3. Vissers, L. E., de Vries, B. B., Osoegawa, K., et al. (2003) Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities. Am. J. Hum. Genet. 73, 1261-1270.