1. Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes;Botta;Am. J. Med. Genet.,1999
2. Mutations in the TWIST gene in the Saethre–Chotzen syndrome;El Ghouzzi;Nat. Genet.,1997
3. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome;Ewart;Nat. Genet.,1993
4. LIM-kinase 1;Frangiskakis;Cell,1996
5. A novel microsatellite DNA marker at locus D7S1870 detects hemizygosity in 75% of patients with Williams syndrome;Gilbert-Dussardier;Am. J. Hum. Genet.,1995