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122 related items for PubMed ID: 2556343
21. Homozygous deletion of a DNA marker from chromosome 11p13 in sporadic Wilms tumor. Lewis WH, Yeger H, Bonetta L, Chan HS, Kang J, Junien C, Cowell J, Jones C, Dafoe LA. Genomics; 1988 Jul; 3(1):25-31. PubMed ID: 2851538 [Abstract] [Full Text] [Related]
23. The chromosome 11 region flanking the t(11;14) breakpoint in human T-ALL is deleted in Wilms' tumor hybrids. Finver SN, Martiniere C, Kagan J, Cavenee W, Croce CM. Oncogene Res; 1989 Jul; 5(2):143-8. PubMed ID: 2558334 [Abstract] [Full Text] [Related]
32. A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids. Glaser T, Housman D, Lewis WH, Gerhard D, Jones C. Somat Cell Mol Genet; 1989 Nov; 15(6):477-501. PubMed ID: 2595451 [Abstract] [Full Text] [Related]
33. Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13. Lavedan C, Barichard F, Azoulay M, Couillin P, Molina Gomez D, Nicolas H, Quack B, Rethoré MO, Noel B, Junien C. Cytogenet Cell Genet; 1989 Nov; 50(2-3):70-4. PubMed ID: 2570677 [Abstract] [Full Text] [Related]