D. Dao

Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors.

B. Tycko, L. Weiss, L. Weiss, 1997, American journal of human genetics.

Deletion of the retinoblastoma gene in multiple myeloma.

B. Barlogie, G. Tricot, J. Sawyer, 1994, Leukemia.

Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor.

W. W. Nichols, L. Strong, S. Pathak, 1987, American journal of human genetics.

Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors.

L. Strong, S. Pathak, V. Riccardi, 1987, American journal of human genetics.

IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes.

B. Tycko, C. Walsh, D. Frank, 1998, Human molecular genetics.

The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis.

B. Tycko, C. Walsh, Q. Wang, 1997, Human molecular genetics.

Studies of BCR and ABL gene rearrangements in chronic myelogenous leukemia patients by conventional and pulsed-field gel electrophoresis using gel inserts.

J. Trujillo, D. Dao, J. Liang, 1989, Cancer genetics and cytogenetics.

Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting.

B. Tycko, C. Walsh, T. Bestor, 1999, Human molecular genetics.