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Risk of sudden death in the Williams-Beuren syndrome.
Wessel A, Gravenhorst V, Buchhorn R, Gosch A, Partsch CJ, Pankau R. Wessel A, et al. Among authors: pankau r. Am J Med Genet A. 2004 Jun 15;127A(3):234-7. doi: 10.1002/ajmg.a.30012. Am J Med Genet A. 2004. PMID: 15150772 Review.
Familial Williams-Beuren syndrome showing varying clinical expression.
Pankau R, Siebert R, Kautza M, Schneppenheim R, Gosch A, Wessel A, Partsch CJ. Pankau R, et al. Am J Med Genet. 2001 Feb 1;98(4):324-9. doi: 10.1002/1096-8628(20010201)98:4<324::aid-ajmg1103>;2-5. Am J Med Genet. 2001. PMID: 11170076 Review.
Chromosome abnormalities and Williams-Beuren syndrome.
Gosch A, Pankau R. Gosch A, et al. Among authors: pankau r. J Med Genet. 1993 Oct;30(10):886. doi: 10.1136/jmg.30.10.886. J Med Genet. 1993. PMID: 8230171 Free PMC article. No abstract available.
Calcium metabolism in Williams-Beuren syndrome.
Kruse K, Pankau R, Gosch A, Wohlfahrt K. Kruse K, et al. Among authors: pankau r. J Pediatr. 1992 Dec;121(6):902-7. doi: 10.1016/s0022-3476(05)80336-1. J Pediatr. 1992. PMID: 1333009
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