|
1
|
Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1.
|
J Med Genet
|
2006
|
2.97
|
|
2
|
Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH.
|
Am J Med Genet A
|
2005
|
1.68
|
|
3
|
15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
|
Clin Genet
|
2006
|
1.09
|
|
4
|
Autism-associated familial microdeletion of Xp11.22.
|
Clin Genet
|
2008
|
1.03
|
|
5
|
Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability.
|
Clin Genet
|
2012
|
0.97
|
|
6
|
Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics.
|
Hum Genet
|
2010
|
0.97
|
|
7
|
Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss.
|
Hum Reprod
|
2010
|
0.95
|
|
8
|
Genomic changes detected by array CGH in human embryos with developmental defects.
|
Mol Hum Reprod
|
2009
|
0.88
|
|
9
|
Putatively benign copy number variants in subjects with idiopathic autism spectrum disorder and/or intellectual disability.
|
Cytogenet Genome Res
|
2009
|
0.75
|
|
10
|
Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability.
|
Am J Med Genet A
|
2009
|
0.75
|