Associated Papers
Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of 300 Indian Patients.
Lall MB et al.
Indian Journal of Pediatrics, 2026
Genome-wide study of copy number variation implicates multiple novel loci for schizophrenia risk in Han Chinese family trios.
Wu X et al.
Iscience, 2021
Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction.
Wesdorp M et al.
Human Genetics, 2018
29754270 (PubMed )
Supplement: 439_2018_1880_MOESM1_ESM.docx
Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects.
Kendall KM et al.
Biological Psychiatry, 2017
Identification of rare copy number variants in high burden schizophrenia families.
Van Den Bossche MJ et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2013
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