Of mice and the fragile X syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference60 articles.
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2. Physical and behavioral phenotype;Hagerman,2002
3. 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
4. Post-mortem examination of two fragile X brothers with an FMR1 full mutation;Reyniers;Am. J. Med. Genet.,1999
5. The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm;Reyniers;Nat. Genet.,1993
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