Genomic microarrays have been implemented in the diagnosis of patients with unexplained mental retardation. This method, although revolutionizing cytogenetics, is still limited to the detection of rare de novo copy number variants (CNVs). Genome-wide single nucleotide polymorphism (SNP) microarrays
✦ LIBER ✦
Array CGH in molecular diagnosis of mental retardation—A study of 150 Finnish patients
✍ Scribed by Linda Siggberg; Sirpa Ala-Mello; Elisa Jaakkola; Esa Kuusinen; Robert Schuit; Jürgen Kohlhase; Detlef Böhm; Jaakko Ignatius; Sakari Knuutila
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 264 KB
- Volume
- 152A
- Category
- Article
- ISSN
- 1552-4825
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