Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiology.

Patsalis, P C; Sismani, C; Hadjimarcou, M I; Rose, N; Stylianidou, G; Koukoulli, R; Anastasiadou, V; Deltas, C C; Middleton, L

Patsalis, P C; Sismani, C; Hadjimarcou, M I; Rose, N; Stylianidou, G; Koukoulli, R; Anastasiadou, V; Deltas, C C; Middleton, L.

Affiliation

Patsalis PC; Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.

Genet Couns ; 8(1): 1-6, 1997.

Article in En | MEDLINE | ID: mdl-9101271

Subject(s)

Fragile X Syndrome/genetics; Intellectual Disability/genetics; Adolescent; Adult; Blotting, Southern; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 11; Chromosomes, Human, Pair 22; Cytogenetics; Humans; Infant; Karyotyping; Point Mutation; Translocation, Genetic

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Collection: 01-internacional Database: MEDLINE Main subject: Fragile X Syndrome / Intellectual Disability Type of study: Etiology_studies Limits: Adolescent / Adult / Child, preschool / Humans / Infant Language: En Journal: Genet Couns Journal subject: ETICA / GENETICA MEDICA Year: 1997 Type: Article Affiliation country: Cyprus

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