Brief psychotic episode in a patient with chromosome 2q37 microdeletion syndrome
Author:
Publisher
BMJ
Subject
General Medicine
Reference10 articles.
1. Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q;Paunio;Hum Mol Genet,2001
2. Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q;Wijsman;Mol Psychiatry,2003
3. Linkage analysis of a completely ascertained sample of familial schizophrenics and bipolars from Palau, Micronesia;Klei;Hum Genet,2005
4. 2q37.3 Deletion Syndrome: Two Cases with Highly Distinctive Facial Phenotype, Discordant Association with Schizophrenic Psychosis, and Shared Deletion Breakpoint Region on 2q37.3;Mehraein;Cytogenet Genome Res,2015
5. Chromosome 2q37 deletion: clinical and molecular aspects;Falk;Am J Med Genet C Semin Med Genet,2007
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Disorders Due to Brain Damage and Dysfunction and to Physical Diseases (Excluding Neurocognitive Disorders);Textbook of Psychiatry for Intellectual Disability and Autism Spectrum Disorder;2022
2. Genotype and phenotype correlation in 103 individuals with 2q37 deletion syndrome reveals incomplete penetrance and supports HDAC4 as the primary genetic contributor;American Journal of Medical Genetics Part A;2019-03-07
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