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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?
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, HRVolume:
120
Language:
english
Journal:
BJOG: An International Journal of Obstetrics & Gynaecology
DOI:
10.1111/1471-0528.12150
Date:
April, 2013
File:
PDF, 125 KB
english, 2013