High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease

Journal of Medical Genetics

Volumn 45, Issue 11, 2008, Pages 704-709

  Erdogan, F ^a   Larsen, L A ^b   Zhang, L ^b   Tumer Z ^b   Tummerup, N ^b   Chen, W ^a   Jacobsen, J R ^c   Schubert, M ^a   Jurkatis, J ^a   Tzschach, A ^a   Ropers, H H ^a   Ullmann, R ^a  

^a MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^b UNIVERSITY OF COPENHAGEN   (Denmark)

^c Rigshospitalet   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 1; CHROMOSOME 17; CHROMOSOME 22; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL HEART DISEASE; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC COUNSELING; GENETIC RISK; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; NEWBORN; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETIC ANALYSIS; FEMALE; GENE DOSAGE; GENE DUPLICATION; GENOME, HUMAN; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; INFANT, NEWBORN; MALE; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PHENOTYPE;

EID: 56049097929     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2008.058776     Document Type: Article

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