Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation.-Reference-Cited by-同舟云学术

Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation.

Published:1992-11-01 Issue:11 Volume:29 Page:794-801
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Heitz D,Devys D,Imbert G,Kretz C,Mandel J L

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference30 articles.

1. Further segregation analysis of the fragile X syndrome with special reference to transmitting males;Sherman, S.L.; Jacobs, P.A.; Morton, N.E.;Hum Genet,1985

2. Instability of a 550 bp DNA segment and abnormal methylation in fragile X syndrome;Oberle, I.; Rousseau, F.; Heitz, D.;Science,1991

3. Fragile X genotype characterized by an unstable region of DNA;Yu, S.; Pritchard, M.; Kremer, E.;Science,1991

4. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CGG)n;Kremer, E.J.; Pritchard, M.; Lynch, M.;Science,1991

5. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk, A.J.; Pieretti, M.; Fu, Y.H.;Cell,1991

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