Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13)
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference26 articles.
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1. Catatonia in Children and Adolescents: A High Rate of Genetic Conditions;Journal of the American Academy of Child & Adolescent Psychiatry;2018-07
2. Prenatal detection and characterization of a psu idic(8)(p23.3) which likely derived from nonallelic homologous recombination between two MYOM2-repeats;Journal of the Formosan Medical Association;2015-01
3. Pre- and postnatal findings in a patient with a novel rec(8)dup(8q)inv(8)(p23.2q22.3) associated with san luis valley syndrome;American Journal of Medical Genetics Part A;2013-07-25
4. Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype;American Journal of Medical Genetics Part A;2013-03-12
5. Molecular cytogenetic characterization and genotype/phenotype analysis in a patient with a de novo 8p23.2p23.3 deletion/12p13.31p13.33 duplication;American Journal of Medical Genetics Part A;2012-05-25
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