Williams–Beuren syndrome: genes and mechanisms

By Francke Uta  

Human Molecular Genetics, Vol. 8, Iss. 10, 1999-10 ,pp. : 1947-1954

Oxford University Press

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

By Tassabehji M.  

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

Oxford University Press

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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

By Merla Giuseppe   Howald Cédric   Antonarakis Stylianos E.   Reymond Alexandre  

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

Oxford University Press

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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

By Cairo S.   Merla G.   Urbinati F.   Ballabio A.   Reymond A.  

Human Molecular Genetics, Vol. 10, Iss. 6, 2001-03 ,pp. : 617-627

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Treacher Collins Syndrome may Result from Insertions, Deletions or Splicing Mutations, Which Introduce a Termination Codon into the Gene

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