Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice

✍ Scribed by Bruno, D L (author);Ganesamoorthy, D (author);Schoumans, J (author);Bankier, A (author);Coman, D (author);Delatycki, M (author);Gardner, R J M (author);Hunter, M (author);James, P A (author);Kannu, P (author);McGillivray, G (author);Pachter, N (author);Peters, H (author);Rieubland, C (author);Savarirayan, R (author);Scheffer, I E (author);Sheffield, L (author);Tan, T (author);White, S M (author);Yeung, A (author);Bowman, Z (author);Ngo, C (author);Choy, K W (author);Cacheux, V (author);Wong, L (author);Amor, D J (author);Slater, H R (author)

• Book ID: 115532946
• Publisher: BMJ
• Year: 2008
• Tongue: English
• Weight: 214 KB
• Volume: 46
• Category: Article
• ISSN: 0022-2593
• DOI: 10.1136/jmg.2008.062604