Paternal Uniparental Isodisomy of the Entire Chromosome 20 as a Molecular Cause of Pseudohypoparathyroidism Type Ib (PHP-Ib)

Por Bastepe, Murat, Altug-Teber, Özge, Agarwal, Chhavi, Oberfield, Sharon E., Bonin, Michael, Jüppner, Harald
Publicado em 2010

Polymorphisms in folate-metabolizing enzymes and response to 5-fluorouracil among stage II or III rectal cancer patients (INT-0144; SWOG 9304)

Por Ulrich, Cornelia M., Rankin, Cathryn, Toriola, Adetunji T., Makar, Karen W., Altug-Teber, Özge, Benedetti, Jacqueline K., Holmes, Rebecca S., Smalley, Stephen R., Blanke, Charles D., Lenz, Heinz-Josef
Publicado no Cancer (2014)