Author:
de Vries B B,Jansen C C,Duits A A,Verheij C,Willemsen R,van Hemel J O,van den Ouweland A M,Niermeijer M F,Oostra B A,Halley D J
Subject
Genetics (clinical),Genetics
Reference20 articles.
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2. Fragile X genotype characterized by an unstable region of DNA;Yu, S.; Pritchard, M.; Kremer, E.;Science,1991
3. Instability of a 550base pair DNA segment and abnormal methylation in fragile X syndrome;Oberle, I.; Rousseau, F.; Heitz, D.;Science,1991
4. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox;Fu, Y.H.; Kuhl, D.P.A.; Pizzutti, A.;Cell,1991
5. Absence of expression of the FMR-1 gene in fragile X syndrome;Pieretti, M.; Zhang, F.; Fu, Y.H.;Cell,1991
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