Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation. | J Med Genet;38(2): 121-5, 2001 Feb. | MEDLINE

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Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation.

Giraudeau, F; Taine, L; Biancalana, V; Delobel, B; Journel, H; Missirian, C; Lacombe, D; Bonneau, D; Parent, P; Aubert, D; Hauck, Y; Croquette, M F; Toutain, A; Mattei, M G; Loiseau, H A; David, A; Vergnaud, G.

J Med Genet ; 38(2): 121-5, 2001 Feb.

Article in En | MEDLINE | ID: mdl-11288712

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 1 / Chromosome Deletion / Microsatellite Repeats / Intellectual Disability Type of study: Diagnostic_studies Limits: Female / Humans / Male Language: En Journal: J Med Genet Year: 2001 Document type: Article

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 1 / Chromosome Deletion / Microsatellite Repeats / Intellectual Disability Type of study: Diagnostic_studies Limits: Female / Humans / Male Language: En Journal: J Med Genet Year: 2001 Document type: Article