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Copy Number and SNP Arrays in Clinical Diagnostics g r o. Christian P. Schaaf, Joanna Wiszniewska, s w e and Arthur L. Beaudet i v e r l . Department of Molecular and Human Genetics, Baylor College of Medicine, a y u l n n Houston, Texas 77030; email: abeaudet@ n o a. e w s u w l w a n o m s o r r e f p d r e o d F a . o 1 l 1 n / w 3 o 1 / D 9 . 0 1 n 5 o - 5 s 2 i Annu. Rev. Genomics Hum. Genet. 2011. 12:25–51 : v Keywords 2 a 1. D 1 - First published online as a Review in Advance on intellectual disability, neuropsychiatric disorders, microarray, 1 a 0 i July 18, 2011 2 n . r mosaicism, consanguinity, prenatal diagnosis t o e f The Annual Review of Genomics and Human Genetics i n l e a is online at G C Abstract n f o a This article’s doi: m y The ability of chromosome microarray analysis (CMA) to detect sub- t u i 10.1146/annurev-genom-092010-110715 s H r microscopic genetic abnormalities has revolutionized the clinical diag- e . v i c m n Copyright
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