B. Pober

Clinical utility gene card for: Williams–Beuren Syndrome [7q11.23]

B. Kozel, U. Koehler, B. Pabst, 2014, European Journal of Human Genetics.

A 1.5 million–base pair inversion polymorphism in families with Williams-Beuren syndrome

Stephen W. Scherer, Lucy R. Osborne, Joann Bodurtha, 2001, Nature Genetics.

Title Hemizygous deletion of the syntaxin 1 A gene in individuals withWilliams syndrome :

B. Pober, SW Tsui T Scherer, 1997 .

Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome.

S. Scherer, L. Tsui, B. Pober, 1997, American journal of human genetics.

Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients.

S. Scherer, H. Heng, L. Tsui, 1996, Genomics.

Control of bone formation by the serpentine receptor Frizzled-9

G. Sauter, K. Knobeloch, U. Francke, 2011, The Journal of cell biology.