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

Bruno, DL (author)

Ganesamoorthy, D (author)

Schoumans, J (author)

Karolinska Institutet

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Bankier, A (author)

Coman, D (author)

Delatycki, M (author)

Gardner, RJM (author)

Hunter, M (author)

James, PA (author)

Kannu, P (author)

McGillivray, G (author)

Pachter, N (author)

Peters, H (author)

Rieubland, C (author)

Savarirayan, R (author)

Scheffer, IE (author)

Sheffield, L (author)

Tan, T (author)

White, SM (author)

Yeung, A (author)

Bowman, Z (author)

Ngo, C (author)

Choy, KW (author)

Cacheux, V (author)

Wong, L (author)

Amor, DJ (author)

Slater, HR (author)

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 (creator_code:org_t)

2008-11-03

2009

English.

In: Journal of medical genetics. - : BMJ. - 1468-6244. ; 46:2, s. 123-131

Related links:

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• Journal article (peer-reviewed)