Cytogenetic versus DNA diagnosis in routine referrais for fragile X syndrome
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference9 articles.
1. The marker (X) chromosome: a cytogenetic and genetic analysis;Sherman;Ann Hum Genet,1984
2. Instability of a 555-base pair DNA segment and abnormal methylation in fragile X syndrome;Oberle;Science,1991
3. Fragile X genotype characterised by an unstable region of DNA;Yu;Science,1991
4. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk;Cell,1991
5. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox;Fu;Cell,1991
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