Identification of complex chromosome 18 rearrangements by FISH and array CGH in two patients with apparent isochromosome 18q

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Veröffentlicht in:American journal of medical genetics. Part A 2011-06, Vol.155A (6), p.1465-1468
Hauptverfasser: Breman, Amy M., Probst, Frank J., Blazo, Maria A., Schaaf, Christian P., Roney, Erin K., Craigen, William J., Bacino, Carlos A., Cheung, Sau Wai
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container_title American journal of medical genetics. Part A
container_volume 155A
creator Breman, Amy M.
Probst, Frank J.
Blazo, Maria A.
Schaaf, Christian P.
Roney, Erin K.
Craigen, William J.
Bacino, Carlos A.
Cheung, Sau Wai
description
doi_str_mv 10.1002/ajmg.a.33935
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Abnormalities, Multiple - genetics
Abnormalities, Multiple - pathology
Biological and medical sciences
Child, Preschool
Chromosomes, Human, Pair 18 - genetics
Comparative Genomic Hybridization
Gene Rearrangement
Heart Defects, Congenital - genetics
Heart Defects, Congenital - pathology
Humans
In Situ Hybridization, Fluorescence
Infant
Isochromosomes - genetics
Karyotyping
Male
Medical genetics
Medical sciences
title Identification of complex chromosome 18 rearrangements by FISH and array CGH in two patients with apparent isochromosome 18q
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