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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1997 | 2 |
1998 | 2 |
2001 | 1 |
2024 | 0 |
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Page 1
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome.
Nat Genet. 2001 Feb;27(2):159-66. doi: 10.1038/84781.
Nat Genet. 2001.
PMID: 11175783
Gpc3 expression correlates with the phenotype of the Simpson-Golabi-Behmel syndrome.
Pellegrini M, Pilia G, Pantano S, Lucchini F, Uda M, Fumi M, Cao A, Schlessinger D, Forabosco A.
Pellegrini M, et al.
Dev Dyn. 1998 Dec;213(4):431-9. doi: 10.1002/(SICI)1097-0177(199812)213:4<431::AID-AJA8>3.0.CO;2-7.
Dev Dyn. 1998.
PMID: 9853964
Free article.
Item in Clipboard
Recombination trapping: an in-vivo approach to recover cDNAs encoded in YACs.
Mazzarella R, Pilia G.
Mazzarella R, et al.
Gene. 1998 Jun 8;212(2):315-22. doi: 10.1016/s0378-1119(98)00109-7.
Gene. 1998.
PMID: 9611273
Item in Clipboard
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) gene.
Huber R, Crisponi L, Mazzarella R, Chen CN, Su Y, Shizuya H, Chen EY, Cao A, Pilia G.
Huber R, et al.
Genomics. 1997 Oct 1;45(1):48-58. doi: 10.1006/geno.1997.4916.
Genomics. 1997.
PMID: 9339360
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Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.
Lindsay S, Ireland M, O'Brien O, Clayton-Smith J, Hurst JA, Mann J, Cole T, Sampson J, Slaney S, Schlessinger D, Burn J, Pilia G.
Lindsay S, et al.
J Med Genet. 1997 Jun;34(6):480-3. doi: 10.1136/jmg.34.6.480.
J Med Genet. 1997.
PMID: 9192268
Free PMC article.
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