Incidental findings on array comparative genomic hybridization: detection of carrier females of dystrophinopathy without any family history.

Nguyen, K; Putoux, A; Busa, T; Cordier, M P; Sigaudy, S; Till, M; Chabrol, B; Michel-Calemard, L; Bernard, R; Julia, S; Malzac, P; Labalme, A; Missirian, C; Edery, P; Popovici, C; Philip, N; Sanlaville, D

Nguyen, K; Putoux, A; Busa, T; Cordier, M P; Sigaudy, S; Till, M; Chabrol, B; Michel-Calemard, L; Bernard, R; Julia, S; Malzac, P; Labalme, A; Missirian, C; Edery, P; Popovici, C; Philip, N; Sanlaville, D.

Affiliation

Nguyen K; Département de Génétique Médicale, Hôpital d'enfants de la Timone, Marseille, France.

Clin Genet ; 87(5): 488-91, 2015 May.

Article in En | MEDLINE | ID: mdl-24835530

Subject(s)

Comparative Genomic Hybridization; Heterozygote; Incidental Findings; Child, Preschool; DNA Copy Number Variations; Dystrophin/genetics; Family; Female; Genetic Counseling; Humans; Infant; Muscular Dystrophies/diagnosis; Muscular Dystrophies/genetics

Key words

X-linked; aCGH; dystrophin; genetic counseling; incidental findings

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Incidental Findings / Comparative Genomic Hybridization / Heterozygote Type of study: Diagnostic_studies / Prognostic_studies Limits: Child, preschool / Female / Humans / Infant Language: En Journal: Clin Genet Year: 2015 Document type: Article

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