Y. Goshen

Clinical relevance of molecular diagnosis in childhood rhabdomyosarcoma.

A. Tobar, S. Avigad, R. Zaizov, 2000, Diagnostic molecular pathology : the American journal of surgical pathology, part B.

Additional chromosome 1q aberrations and der(16)t(1;16), correlation to the phenotypic expression and clinical behavior of the Ewing family of tumors

I. Cohen, R. Zaizov, S. Ash, 2004, Journal of Neuro-Oncology.

High frequency of loss of heterozygosity for 1p35-p36 (D1S247) in Wilms tumor.

S. Avigad, R. Zaizov, S. Ash, 2000, Cancer genetics and cytogenetics.

Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygous.

H. Tamary, E. Girodon, F. Galactéros, 1994, Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.

Methotrexate Treatment Protocols and the Central Nervous System: Significant Cure With Significant Neurotoxicity

I. Yaniv, A. Shuper, L. Kornreich, 2000, Journal of child neurology.

PAX3/forkhead homolog in rhabdomyosarcoma oncoprotein activates glucose transporter 4 gene expression in vivo and in vitro.

D. Esposito, M. Quon, I. Yaniv, 2002, The Journal of clinical endocrinology and metabolism.