Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?

✍ Scribed by Ganesamoorthy, D; Bruno, DL; McGillivray, G; Norris, F; White, SM; Adroub, S; Amor, DJ; Yeung, A; Oertel, R; Pertile, MD; Ngo, C; Arvaj, AR; Walker, S; Charan, P; Palma-Dias, R; Woodrow, N; Slater, HR

• Book ID: 120526503
• Publisher: John Wiley and Sons
• Year: 2013
• Tongue: English
• Weight: 125 KB
• Volume: 120
• Category: Article
• ISSN: 1470-0328
• DOI: 10.1111/1471-0528.12150