Autism-associated familial microdeletion of Xp11.22
Qiao, Y, Liu, X, Harvard, C, Hildebrand, MJ, Rajcan-Separovic, E, Holden, JJA, Lewis, MES
Published in Clinical genetics (01.08.2008)
Published in Clinical genetics (01.08.2008)
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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
Harvard, C, Malenfant, P, Koochek, M, Creighton, S, Mickelson, ECR, Holden, JJA, Lewis, MES, Rajcan-Separovic, E
Published in Clinical genetics (01.04.2005)
Published in Clinical genetics (01.04.2005)
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A new frontier for fetal diagnosis using genomic CGH microarrays
Published in Clinical genetics
(01.02.2005)
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Journal Article
Higher resolution solutions for mapping the mystery of idiopathic intellectual disability
Published in Clinical genetics
(01.02.2005)
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Journal Article
Melding mind and matter in gene expression studies of the human brain
Published in Clinical genetics
(01.09.2004)
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Journal Article
Simplifying the complex genetics of schizophrenia
Published in Clinical genetics
(01.09.2004)
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Journal Article
Face-brain asymmetry in autism spectrum disorders
Hammond, P, Forster-Gibson, C, Chudley, A E, Allanson, J E, Hutton, T J, Farrell, S A, McKenzie, J, Holden, J J A, Lewis, M E S
Published in Molecular psychiatry (01.06.2008)
Published in Molecular psychiatry (01.06.2008)
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Autism severity is associated with child and maternal MAOA genotypes
Cohen, IL, Liu, X, Lewis, MES, Chudley, A, Forster-Gibson, C, Gonzalez, M, Jenkins, EC, Brown, WT, Holden, JJA
Published in Clinical genetics (01.04.2011)
Published in Clinical genetics (01.04.2011)
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