![](/img/cover-not-exists.png)
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
C Harvard, P Malenfant, M Koochek, S Creighton, ECR Mickelson, JJA Holden, MES Lewis, E Rajcan-SeparovicVolume:
67
Year:
2005
Language:
english
Pages:
11
DOI:
10.1111/j.1399-0004.2005.00406.x
File:
PDF, 1.62 MB
english, 2005