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Diagnostic yield of chromosomal microarray and trio whole exome sequencing in congenital brain anomalies
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- Journal:
- European Psychiatry / Volume 66 / Issue S1 / March 2023
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- 19 July 2023, p. S887
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Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability
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- European Psychiatry / Volume 66 / Issue S1 / March 2023
- Published online by Cambridge University Press:
- 19 July 2023, p. S887
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Identification of candidate genes of intellectual disability by single-gene deletions/amplifications mapping using chromosomal microarray analysis
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- European Psychiatry / Volume 65 / Issue S1 / June 2022
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- 01 September 2022, p. S382
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Concomitant CNVs in healthy carriers with 7q31.1 microdeletions may suppress intellectual disability and autism spectrum disorders phenotype
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- European Psychiatry / Volume 65 / Issue S1 / June 2022
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- 01 September 2022, p. S382
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EPA-0644 - 3p26.3 - Candidate Loci of Intellectual Disability
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- European Psychiatry / Volume 29 / Issue S1 / 2014
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- 15 April 2020, p. 1
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1866 – Novel Candidate Genomic Loci For Mental Retardation
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- European Psychiatry / Volume 28 / Issue S1 / 2013
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- 15 April 2020, 28-E1114
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Concomitant 3q13.31 Microdeletion and Ring Chromosome 22 in a Patient with Severe Developmental Delay, Ventriculomegaly, and Dandy-walker Malformation
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- European Psychiatry / Volume 41 / Issue S1 / April 2017
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- 23 March 2020, p. S167
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