Işık Bökesoy

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome

Yanyan Jiang, Muriel Rigolet, Déborah Bourc’his et al. · Human Mutation · 2004 · 133 citations

Life Sciences, Genetics, Molecular Genetics +17

Urinary cyclophosphamide excretion and micronuclei frequencies in peripheral lymphocytes and in exfoliated buccal epithelial cells of nurses handling antineoplastics

Sema Burgaz, Bensu Karahalıl, Pinar Bayrak et al. · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · 1999 · 123 citations

Medicine, Oncology, Oncology Nursing +8

Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease.

Toydemir Pb, Atilla Halil Elhan, Ajlan Tükün et al. · PubMed · 2000 · 57 citations

Medicine, Genetics, Hematology +17

Butterfly vertebra: A case report

Birkan Sonel, Peyman Yalçın, Erhan Arif Öztürk et al. · Clinical Imaging · 2001 · 39 citations

Medicine, Anatomy, Clinical Anatomy +12

Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser syndrome in a girl with 46,X,del(X)(pter→q22:)

Sena Aydos, Ajlan Tükün, Işık Bökesoy · Archives of Gynecology and Obstetrics · 2003 · 37 citations

Medicine, Genetics, Molecular Genetics +14