Array CGH in molecular diagnosis of mental retardation-A study of 150 Finnish patients

We report on the results of an array comparative genomic hybridization (array CGH) study of 150 karyotypically normal Finnish patients with idiopathic mental retardation and/or dysmorphic features and/or malformations. Using high‐resolution microarray analysis, we sought to identify clinically relev...

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Veröffentlicht in:	American journal of medical genetics. Part A 2010-06, Vol.152A (6), p.1398-1410
Hauptverfasser:	Siggberg, Linda, Ala-Mello, Sirpa, Jaakkola, Elisa, Kuusinen, Esa, Schuit, Robert, Kohlhase, Jürgen, Böhm, Detlef, Ignatius, Jaakko, Knuutila, Sakari
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Adult and adolescent clinical studies array CGH Biological and medical sciences Child Child, Preschool Chromosomes, Human, X - genetics Comparative Genomic Hybridization - methods deletion duplication Female Finland Gene Duplication Humans Infant Intellectual deficiency Intellectual Disability - diagnosis Intellectual Disability - genetics Male Medical genetics Medical sciences mental retardation Oligonucleotide Array Sequence Analysis - methods Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Sequence Deletion
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