High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results

BMC Medical Genetics

Volumn 13, Issue , 2012, Pages

  Siggberg, Linda ^a   Sirpa, Ala Mello ^b   Tarja, Linnankivi ^c   Kristiina, Avela ^d   Ilari, Scheinin ^a,e,g   Kati, Kristiansson ^f,g   Päivi, Lahermo ^g   Marja, Hietala ^h   Liisa, Metsähonkala ^c   Esa, Kuusinen ⁱ   Maarit, Laaksonen ^f   Janna, Saarela ^g   Sakari, Knuutila ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

^b Rinnekoti Foundation Finland   (Finland)

^c HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^d Department of Medical Genetics ^*  (Finland)

^e VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^f NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

^g UNIVERSITY OF HELSINKI   (Finland)

^h TURKU UNIVERSITY HOSPITAL   (Finland)

ⁱ Satakunta Hospital District   (Finland)

Author keywords

Developmental disorder; Diagnostic yield; SNP array

Indexed keywords

ALLELE; ARTICLE; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; COPY NUMBER VARIATION; DEVELOPMENTAL DISORDER; HOMOZYGOSITY; HUMAN; PHENOTYPE; SINGLE NUCLEOTIDE POLYMORPHISM;

COMPARATIVE GENOMIC HYBRIDIZATION; DEVELOPMENTAL DISABILITIES; DNA COPY NUMBER VARIATIONS; HOMOZYGOTE; HUMANS; MICROSATELLITE REPEATS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; UNIPARENTAL DISOMY;

EID: 84866159075     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-13-84     Document Type: Article

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