Pure partial trisomy 4q syndrome in a child with der(9)ins(9;4)(q34.3;q26q35.2)mat.

Topcu, V; Ilgin-Ruhi, H; Yurur-Kutlay, N; Ekici, C; Vicdan, A; Tukun, F A

Topcu, V; Ilgin-Ruhi, H; Yurur-Kutlay, N; Ekici, C; Vicdan, A; Tukun, F A.

Genet Couns ; 25(1): 1-6, 2014.

Article in En | MEDLINE | ID: mdl-24783648

Subject(s)

Abnormalities, Multiple/genetics; Developmental Disabilities/genetics; Language Development Disorders/genetics; Polydactyly/genetics; Trisomy; Abnormalities, Multiple/pathology; Adult; Child, Preschool; Chromosomes, Human, Pair 4/genetics; Chromosomes, Human, Pair 9/genetics; Developmental Disabilities/pathology; Developmental Disabilities/physiopathology; Female; Humans; In Situ Hybridization, Fluorescence; Karyotype; Language Development Disorders/pathology; Language Development Disorders/physiopathology; Magnetic Resonance Imaging; Male; Polydactyly/pathology; Trisomy/genetics; Trisomy/pathology; Trisomy/physiopathology

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Collection: 01-internacional Database: MEDLINE Main subject: Trisomy / Abnormalities, Multiple / Developmental Disabilities / Polydactyly / Language Development Disorders Limits: Adult / Child, preschool / Female / Humans / Male Language: En Journal: Genet Couns Journal subject: ETICA / GENETICA MEDICA Year: 2014 Document type: Article Country of publication: Switzerland

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