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Article

Array-based genomic delineation of a familial duplication 11q14.1-q22.1 associated with recurrent depression.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 5 Apr 2006

Kolomietz Elena, Ben-Omran Tawfeg, Chitayat David, Mah Mimi, Murphy Jillian, Nie Gloria, Teshima Ikuko

Abstract excerpt

Detection of abnormal karyotypes with associated clinical manifestations is an important tool for the identification of genes that confer susceptibility to genetic disorders. We present a family with a duplication 11q14.1-q22.1 resulting from an unbalanced familial insertion, associated with a mild dysmorphic phenotype and mood disorders, mainly major depression. This relatively large duplication of a segment...

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PMID: 16526031
DOI: 10.1002/ajmg.b.30297

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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