Tightly linked polymorphic markers for fragile X syndrome and prenatal cytogenetic diagnostic experience.

Glass, I A; Del Mastro, R G; Lanyon, W G; Raeburn, J A; Kilpatrick, M W; Webb, T P; Connor, J M

Glass, I A; Del Mastro, R G; Lanyon, W G; Raeburn, J A; Kilpatrick, M W; Webb, T P; Connor, J M.

Affiliation

Glass IA; Dept of Clinical Genetics, University of Birmingham.

Am J Med Genet ; 43(6): 1050-6, 1992 Aug 01.

Article in En | MEDLINE | ID: mdl-1415337

Subject(s)

Fragile X Syndrome/genetics; Cytogenetics; DNA/genetics; Female; Fragile X Syndrome/diagnosis; Genetic Carrier Screening; Genetic Linkage; Genetic Markers; Humans; Male; Polymorphism, Genetic; Pregnancy; Prenatal Diagnosis

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Collection: 01-internacional Database: MEDLINE Main subject: Fragile X Syndrome Type of study: Diagnostic_studies Limits: Female / Humans / Male / Pregnancy Language: En Journal: Am J Med Genet Year: 1992 Type: Article

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