Williams–Beuren syndrome: a challenge for genotype–phenotype correlations

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Human Molecular Genetics, Vol. 12, Iss. 2, 2003-10 ,pp. : 229-237

Oxford University Press

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Rare genomic rearrangement in a boy with Williams–Beuren syndrome associated to XYY syndrome and intriguing behavior

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The subcellular localization of the ChoRE-binding protein, encoded by the Williams–Beuren syndrome critical region gene 14, is regulated by 14-3-3

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Human Molecular Genetics, Vol. 13, Iss. 14, 2004-07 ,pp. : 1505-1514

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WBSCR14 , a gene mapping to the Williams–Beuren syndrome deleted region, is a new member of the Mlx transcription factor network

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Unequal Interchromosomal Rearrangements May Result in Elastin Gene Deletions Causing the Williams-Beuren syndrome

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