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TypeTitleAuthor(s)YearViews
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndromeOsborne, LR; Li, M; Pober, B; Chitayat, D; Bodurtha, J; Mandel, A; Costa, T; Grebe, T; Cox, S; Tsui, LC; Scherer, SW20011,777
 
Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome: Letters to the editorOsborne, LR; Soder, S; Shi, XM; Pober, B; Costa, T; Scherer, SW; Tsui, L-C1997295
 
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patientsOsborne, LR; Martindale, D; Scherer, SW; Shi, XM; Huizenga, J; Heng, HHQ; Costa, T; Pober, B; Lew, L; Brinkman, J; Rommens, J; Koop, B; Tsui, LC1996284
 
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