Detection of an unusual 17p13.3 microdeletion by array comparative genomic hybridisation in a patient with lissencephaly.

Chabchoub, E; de Ravel, T; Thoelen, R; Vermeesch, J R; Fryns, J-P; Van Esch, H

Chabchoub, E; de Ravel, T; Thoelen, R; Vermeesch, J R; Fryns, J-P; Van Esch, H.

Clin Genet ; 70(6): 535-7, 2006 Dec.

Article in En | MEDLINE | ID: mdl-17101002

Subject(s)

Brain/abnormalities; Chromosome Deletion; Chromosome Disorders/genetics; Chromosomes, Human, Pair 17/genetics; Phenotype; Belgium; Brain/pathology; Child; Female; Humans; In Situ Hybridization, Fluorescence; Nucleic Acid Hybridization

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Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Chromosomes, Human, Pair 17 / Brain / Chromosome Deletion / Chromosome Disorders Type of study: Diagnostic_studies Limits: Child / Female / Humans Country/Region as subject: Europa Language: En Journal: Clin Genet Year: 2006 Document type: Article

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