17q21.31 microdeletion syndrome: further expanding the clinical phenotype.

Sharkey, F H; Morrison, N; Murray, R; Iremonger, J; Stephen, J; Maher, E; Tolmie, J; Jackson, A P

Sharkey, F H; Morrison, N; Murray, R; Iremonger, J; Stephen, J; Maher, E; Tolmie, J; Jackson, A P.

Affiliation

Sharkey FH; Western General Hospital, Edinburgh, UK. freddie.sharkey@luht.scot.nhs.uk

Cytogenet Genome Res ; 127(1): 61-6, 2009.

Article in En | MEDLINE | ID: mdl-20110647

Subject(s)

Abnormalities, Multiple/genetics; Chromosome Deletion; Chromosomes, Human, Pair 17; Adolescent; Child, Preschool; Craniofacial Abnormalities/genetics; Female; Humans; In Situ Hybridization, Fluorescence; Learning Disabilities/genetics; Male; Muscle Hypotonia/genetics; Phenotype; Young Adult

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 17 / Chromosome Deletion Type of study: Risk_factors_studies Limits: Adolescent / Adult / Child, preschool / Female / Humans / Male Language: En Journal: Cytogenet Genome Res Year: 2009 Document type: Article

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