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Title
Adult expression of a 3q13.31 microdeletion
Authors
Keywords
3q13 deletion, Schizophrenia, Copy number variation, Genotype-phenotype correlation, Genetic counselling, Genomic disorder, Nonverbal learning disability
Journal
Molecular Cytogenetics
Volume 7, Issue 1, Pages 23
Publisher
Springer Nature
Online
2014-03-21
DOI
10.1186/1755-8166-7-23
References
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- A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features
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- Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
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