Mosaicism for combined tetrasomy of chromosomes 8 and 18 in a dysmorphic child: A result of failed tetraploidy correction?

BMC Medical Genetics

Volumn 10, Issue , 2009, Pages

  Houge, Gunnar ^a,b   Lybæk, Helle ^a   Gulati, Sasha ^c  

^a HAUKELAND UNIVERSITY HOSPITAL   (Norway)

^b UNIVERSITY OF BERGEN   (Norway)

^c Alesund Hospital   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

CELL DNA;

AORTA COARCTATION; ARTICLE; AUDIOMETRY; CASE REPORT; CHILD; CHROMOSOME 18; CHROMOSOME 8; CHROMOSOME ABERRATION; CHROMOSOME G BAND; CHROMOSOME MOSAICISM; CHROMOSOME PAIRING; COMPARATIVE GENOMIC HYBRIDIZATION; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL MALFORMATION; CYTOKINESIS; EAR MALFORMATION; EMBRYO DEVELOPMENT; EYE EXAMINATION; FACE DYSMORPHIA; FEEDING DISORDER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOOT MALFORMATION; GASTROSTOMY; HEAD CIRCUMFERENCE; HEARING LOSS; HEART SURGERY; HEART VENTRICLE SEPTUM DEFECT; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPING; LANGUAGE DISABILITY; LEUKOCYTE CULTURE; MITOTIC MALSEGREGATION; MITOTIC SLIPPAGE; NEWBORN; PATENT DUCTUS ARTERIOSUS; PHENOTYPE; PRESCHOOL CHILD; PSYCHOMOTOR RETARDATION; RETINA DISEASE; SHORT STATURE; TETRAPLOIDY; TETRASOMY; ALLELE; ANEUPLOIDY; GENETICS; INFANT; MOSAICISM; MULTIPLE MALFORMATION SYNDROME; NONDISJUNCTION; TANDEM REPEAT;

ABNORMALITIES, MULTIPLE; ALLELES; ANEUPLOIDY; CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, HUMAN, PAIR 8; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MOSAICISM; NONDISJUNCTION, GENETIC; PHENOTYPE; TANDEM REPEAT SEQUENCES;

EID: 66649131777     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-10-42     Document Type: Article

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