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, HR
Published in BJOG : an international journal of obstetrics and gynaecology (01.04.2013)
Published in BJOG : an international journal of obstetrics and gynaecology (01.04.2013)
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