[Deletion of 17p11.2 chromosome in Spanish families with hereditary neuropathy and abnormal sensitivity to pressure].

Pou Serradell, A; Espadaler, J M; Aragonés, J M; Bufill, E; Alameda, F; Vílchez, J J; Sevilla, T; Piqueras, A; Palau, F; Bort, S

[Deletion of 17p11.2 chromosome in Spanish families with hereditary neuropathy and abnormal sensitivity to pressure]. / Deleción del cromosoma 17p11.2 en familias españolas con neuropatía hereditaria por vulnerabilidad excesiva a la presión.

Pou Serradell, A; Espadaler, J M; Aragonés, J M; Bufill, E; Alameda, F; Vílchez, J J; Sevilla, T; Piqueras, A; Palau, F; Bort, S.

Affiliation

Pou Serradell A; Servicio de Neurología, Hospital Universitario del Mar, Barcelona.

Neurologia ; 10(9): 367-74, 1995 Nov.

Article in Es | MEDLINE | ID: mdl-8554792

Subject(s)

Chromosome Deletion; Chromosomes, Human, Pair 17; Hereditary Sensory and Motor Neuropathy/genetics; Adult; Aged; Chromosome Aberrations; Chromosome Disorders; Electromyography; Female; Foot Deformities/genetics; Hereditary Sensory and Motor Neuropathy/physiopathology; Humans; Male; Middle Aged; Pedigree; Peripheral Nerves/physiopathology; Sural Nerve/physiopathology; Sural Nerve/ultrastructure

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Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 17 / Hereditary Sensory and Motor Neuropathy / Chromosome Deletion Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: Es Journal: Neurologia Journal subject: NEUROLOGIA Year: 1995 Type: Article

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