Etiological yield of SNP microarrays in idiopathic intellectual disability

European Journal of Paediatric Neurology

Volumn 18, Issue 3, 2014, Pages 327-337

  Utine, G Eda ^a   Haliloǧlu, Göknur ^a   Volkan Salanci, Bilge ^a   Çetinkaya, Arda ^a   Kiper, Pelin Ö ^a   Alanay, Yasemin ^a   Aktaş, Dilek ^a   Anlar, Banu ^a   Topçu, Meral ^a   Boduroǧlu, Koray ^a   Alikaşifoǧlu, Mehmet ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

FOXP2; Intellectual disability; NRXN1; SNP microarray; Subtelomeric rearrangements; UBE2A; Uniparental disomy

Indexed keywords

TRANSCRIPTION FACTOR FOXP2;

ADOLESCENT; ADULT; ANALYTICAL EQUIPMENT; ARTICLE; CEREBELLUM ATROPHY; CHILD; CORPUS CALLOSUM AGENESIS; DISEASE SEVERITY; FEMALE; GENE DELETION; GENE DOSAGE; HAPPY PUPPET SYNDROME; HOMOZYGOSITY; HUMAN; IDIOPATHIC INTELLECTUAL DISABILITY; INTELLECTUAL IMPAIRMENT; LEUKOMALACIA; MAJOR CLINICAL STUDY; MALE; MEDICAL HISTORY; MICROARRAY ANALYSIS; PRIORITY JOURNAL; PSYCHOMETRY; SEIZURE; SINGLE NUCLEOTIDE POLYMORPHISM; SOCIAL INTERACTION; UNIPARENTAL DISOMY; COPY NUMBER VARIATION; ETIOLOGY; GENETIC PREDISPOSITION; GENETIC SCREENING; GENETICS; PRESCHOOL CHILD; PROCEDURES; YOUNG ADULT;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; HUMANS; INTELLECTUAL DISABILITY; MALE; MICROARRAY ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; UNIPARENTAL DISOMY; YOUNG ADULT;

EID: 84900333689     PISSN: 10903798     EISSN: 15322130     Source Type: Journal    
DOI: 10.1016/j.ejpn.2014.01.004     Document Type: Article

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