Recurrent Williams-Beuren Syndrome in a Sibship Suggestive of Maternal Germ-Line Mosaicism Ali Kara-Mostefa, Odile Raoul, Stanislas Lyonnet, Jeanne Amiel,

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Recurrent Williams-Beuren Syndrome in a Sibship Suggestive of Maternal Germ-Line Mosaicism Ali Kara-Mostefa, Odile Raoul, Stanislas Lyonnet, Jeanne Amiel, Arnold Munnich, Michel Vekemans, Suzel Magnier, Batool Ossareh, Jean-Paul Bonnefont The American Journal of Human Genetics Volume 64, Issue 5, Pages 1475-1478 (May 1999) DOI: 10.1086/302362 Copyright © 1999 The American Society of Human Genetics Terms and Conditions

Figure 1 Photograph of the affected siblings The American Journal of Human Genetics 1999 64, 1475-1478DOI: (10.1086/302362) Copyright © 1999 The American Society of Human Genetics Terms and Conditions

Figure 2 Segregation of microsatellite polymorphic markers within and surrounding the elastin gene on chromosome 7q in the nuclear family. The markers used and approximate genetic distances are given in the inset (sex average). The (CA)n repeat, which occurs in the elastin gene intron 18; marker D7S489B; and marker D7S1870 are known to be deleted in typical WS. The American Journal of Human Genetics 1999 64, 1475-1478DOI: (10.1086/302362) Copyright © 1999 The American Society of Human Genetics Terms and Conditions