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Items: 3

1.
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
A Koufos, P Grundy, K Morgan, K A Aleck, T Hadro, B C Lampkin, A Kalbakji, W K Cavenee
Am J Hum Genet. 1989 May; 44(5): 711–719.
PMCID:
PMC1715635
ArticlePDF–1.4M
2.
A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.
J A Crolla, J E Cawdery, C A Oley, I D Young, J Gray, J Fantes, V van Heyningen
J Med Genet. 1997 Mar; 34(3): 207–212. doi: 10.1136/jmg.34.3.207
PMCID:
PMC1050894
ArticlePDF–1.3M
3.
Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells.
A E Reeve, S A Sih, A M Raizis, A P Feinberg
Mol Cell Biol. 1989 Apr; 9(4): 1799–1803. doi: 10.1128/mcb.9.4.1799
PMCID:
PMC362601
ArticlePDF–1.4M

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