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

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 141 B, Issue 3, 2006, Pages 214-219

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

^a UNIVERSITY OF TORONTO   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

Duplication 11q; Familial chromosomal imbalance; Mood disorder

Indexed keywords

ADULT; ARTICLE; CHROMOSOME 11Q; CHROMOSOME DUPLICATION; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; ENVIRONMENTAL FACTOR; FEMALE; GENE EXPRESSION; GENE IDENTIFICATION; GENE INSERTION; GENE MAPPING; GENETIC SUSCEPTIBILITY; HUMAN; HUMAN CELL; INFANT; KARYOTYPE; MAJOR DEPRESSION; MALE; MOOD DISORDER; PRIORITY JOURNAL;

ADOLESCENT; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 9; DEPRESSIVE DISORDER; FAMILY HEALTH; FEMALE; GENE DUPLICATION; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; NUCLEIC ACID HYBRIDIZATION; PEDIGREE; RECURRENCE; SEQUENCE ANALYSIS, DNA; SPECTRAL KARYOTYPING;

EID: 33645964275     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.30297     Document Type: Article

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