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Your search keyword '"Brueton, L."' showing total 26 results

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1. Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data

4. Mutation update for theCSB/ERCC6andCSA/ERCC8genes involved in Cockayne syndrome

5. Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype

13. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

17. Clinical and hematologic aspects of the X-linked α-thalassemia/mental retardation syndrome (ATR-X)

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