Considering specific clinical features as evidence of pathogenic copy number variants.

Preiksaitiene, Egle; Molyte, Alma; Kasnauskiene, Jurate; Ciuladaite, Zivile; Utkus, Algirdas; Patsalis, Philippos C; Kucinskas, Vaidutis

Preiksaitiene, Egle; Molyte, Alma; Kasnauskiene, Jurate; Ciuladaite, Zivile; Utkus, Algirdas; Patsalis, Philippos C; Kucinskas, Vaidutis.

Affiliation

Preiksaitiene E; Department of Human and Medical Genetics, Faculty of Medicine, Vilnius University, Santariskiu st. 2, 08661, Vilnius, Lithuania, eglepreiksaitiene@gmail.com.

J Appl Genet ; 55(2): 189-96, 2014 May.

Article in En | MEDLINE | ID: mdl-24535828

Subject(s)

DNA Copy Number Variations/genetics; Adolescent; Child; Child, Preschool; Chromosome Aberrations; Cluster Analysis; Developmental Disabilities/genetics; Female; Humans; Infant; Intellectual Disability/genetics; Logistic Models; Male; Multivariate Analysis; Translocation, Genetic; Young Adult

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Copy Number Variations Type of study: Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: J Appl Genet Journal subject: GENETICA Year: 2014 Document type: Article Country of publication: United kingdom

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