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1. Characterization of Fxr1 in Danio rerio; a simple vertebrate model to study costamere development


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2. β-catenin tyrosine 654 phosphorylation increases Wnt signalling and intestinal tumorigenesis


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3. Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21.

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4. Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1).

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5. Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1).


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6. Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus


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7. Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.

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8. High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridization.

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9. Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia.

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10. The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion

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