Cytogenetic diagnosis of the fragile X syndrome: efficiency, utilization, and trends.

Shapiro, L R; Wilmot, P L; Shapiro, D A; Pettersen, I M; Casamassima, A C

Shapiro, L R; Wilmot, P L; Shapiro, D A; Pettersen, I M; Casamassima, A C.

Affiliation

Shapiro LR; Department of Pediatrics, New York Medical College, Valhalla.

Am J Med Genet ; 38(2-3): 408-10, 1991.

Article in En | MEDLINE | ID: mdl-2018082

Subject(s)

Fragile X Syndrome/diagnosis; Genetic Techniques; Genetic Testing; Evaluation Studies as Topic; Female; Fragile X Syndrome/genetics; Genetic Techniques/statistics & numerical data; Genetic Techniques/trends; Genetic Testing/statistics & numerical data; Genetic Testing/trends; Humans; Intellectual Disability/diagnosis; Intellectual Disability/genetics; Male

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Collection: 01-internacional Database: MEDLINE Main subject: Genetic Testing / Genetic Techniques / Fragile X Syndrome Type of study: Diagnostic_studies / Evaluation_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Am J Med Genet Year: 1991 Type: Article

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