Array comparative genomic hybridization as a clinical diagnostic tool in syndromic and nonsyndromic congenital heart disease

Pediatric Research

Volumn 73, Issue 6, 2013, Pages 772-776

  Syrmou, Areti ^a   Tzetis, Maria ^a   Fryssira, Helen ^a   Kosma, Konstantina ^a   Oikonomakis, Vasilis ^a   Giannikou, Krinio ^a,b   Makrythanasis, Periklis ^a,c   Kitsiou Tzeli, Sophia ^a   Kanavakis, Emmanuel ^a,b  

^a UNIVERSITY OF ATHENS MEDICAL SCHOOL   (Greece)

^b Children's Hospital   (Greece)

^c UNIVERSITY OF GENEVA   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL HEART DISEASE; CONGENITAL MALFORMATION; COPY NUMBER VARIATION; DIAGNOSTIC TEST; FEMALE; GENE REARRANGEMENT; GENETIC COUNSELING; GENOTYPE PHENOTYPE CORRELATION; HUMAN; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; MALE; MICROARRAY ANALYSIS; MUSCLE HYPOTONIA; NUCLEAR MAGNETIC RESONANCE IMAGING; OLIGONUCLEOTIDE PROBE; PHENOTYPIC VARIATION; PRIORITY JOURNAL; SEIZURE;

COMPARATIVE GENOMIC HYBRIDIZATION; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; INFANT, NEWBORN; SYNDROME;

EID: 84878176890     PISSN: 00313998     EISSN: 15300447     Source Type: Journal    
DOI: 10.1038/pr.2013.41     Document Type: Article

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