[A case of 9p-syndrome identified chromosome 20 on chromosome 9p by M-FISH].

Koseki, N; Obara, Y; Ookawa, A; Katsumi, M; Funato, T; Kaku, M

Koseki, N; Obara, Y; Ookawa, A; Katsumi, M; Funato, T; Kaku, M.

Affiliation

Koseki N; Clinical Labratory, Tohoku University Hospital, Sendai 980-8574.

Rinsho Byori ; 49(10): 1045-8, 2001 Oct.

Article in Ja | MEDLINE | ID: mdl-11769470

Subject(s)

Abnormalities, Multiple/genetics; Chromosomes, Human, Pair 20/genetics; Chromosomes, Human, Pair 9/genetics; Chromosome Deletion; Craniofacial Abnormalities/genetics; Diagnosis, Differential; Female; Humans; In Situ Hybridization, Fluorescence; Infant; Syndrome

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Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 9 / Chromosomes, Human, Pair 20 Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Infant Language: Ja Journal: Rinsho Byori Year: 2001 Document type: Article

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