|
|||||
|
|
A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH |
|
| Authors: | Harvard C Malenfant P Koochek M Creighton S Mickelson E C R Holden J J A Lewis M E S Rajcan-Separovic E |
| Affiliation: | Department of Pathology, University of British Columbia, Vancouver, British Columbia, Canada. |
| Abstract: | |
| Keywords: | array comparative genomic hybridization autism spectrum disorder Cri du Chat syndrome cytogenetics microarray microdeletions in de novo rearrangements microsatellite analysis phenotype–genotype correlation polymorphisms |
| 本文献已被 PubMed 等数据库收录！ | |