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American Journal of Medical Genetics|July 12, 1996
Refinement of the background genetic map of Xq26-q27 and gene localisation for Börjeson-Forssman-Lehmann SyndromeA K Gedeon, H M Kozman, H Robinson, et al.Genome Research|January 1, 1997
4.5-Mb YAC STS contig at 50-kb resolution, spanning Xq25 deletions in two patients with lymphoproliferative syndromeG Porta, S MacMillan, R Nagaraja, et al.Developmental Dynamics : an Official Publication of the American Association of Anatomists|December 16, 1998
Gpc3 expression correlates with the phenotype of the Simpson-Golabi-Behmel syndromeM Pellegrini, G Pilia, S Pantano, et al.Genomics|November 1, 1993
ZNF75: isolation of a cDNA clone of the KRAB zinc finger gene subfamily mapped in YACs 1 Mb telomeric of HPRTA Villa, I Zucchi, G Pilia, et al.Genomics|October 27, 1997
Analysis of exon/intron structure and 400 kb of genomic sequence surrounding the 5'-promoter and 3'-terminal ends of the human glypican 3 (GPC3) geneR Huber, L Crisponi, R Mazzarella, et al.Proceedings of the National Academy of Sciences of the United States of America|January 20, 1999
DNA methylation in transcriptional repression of two differentially expressed X-linked genes, GPC3 and SYBL1R Huber, R S Hansen, M Strazzullo, et al.Nature Genetics|March 1, 1996
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndromeG Pilia, R M Hughes-Benzie, A MacKenzie, et al.Human Genetics|January 1, 1996
Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1D Trump, G Pilia, P H Dixon, et al.Nature Genetics|July 11, 2000
Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28P Taillon-Miller, I Bauer-Sardiña, N L Saccone, et al.American Journal of Human Genetics|August 1, 1997
A submicroscopic deletion in Xq26 associated with familial situs ambiguusG B Ferrero, M Gebbia, G Pilia, et al.Pageof 4