S. Cingoz

发表

A novel subtype of distal symphalangism affecting only the 4th finger

S. Mundlos, N. Tommerup, K. Kjaer, 2009, American journal of medical genetics. Part A.

An excess of chromosome 1 breakpoints in male infertility

R. Stallings, C. Lundsteen, Z. Tümer, 2004, European Journal of Human Genetics.

A novel missense mutation (N78D) in a family with von Hippel–Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts

R. Luijt, M. Apaydin, E. Kurt, 2013, Familial Cancer.

DNA copy number changes detected by comparative genomic hybridization and their association with clinicopathologic parameters in breast tumors.

S. Saydam, T. Canda, M. Sakızlı, 2003, Cancer genetics and cytogenetics.

4q35 deletion and 10p15 duplication associated with immunodeficiency

Z. Tümer, N. Tommerup, H. Ropers, 2006, American journal of medical genetics. Part A.

Identification of the variations in the CPT1B and CHKB genes along with the HLA-DQB1*06:02 allele in Turkish narcolepsy patients and healthy persons.

A. Evlice, H. Yılmaz, Ibrahim Oztura, 2014, Genetic testing and molecular biomarkers.

Novel biallelic variants affecting the OTU domain of the gene OTUD6B associate with severe intellectual disability syndrome and molecular dynamics simulations.

Bradley P. Coe, B. Coe, E. Eichler, 2022, European journal of medical genetics.

Novel anti-HER2 monoclonal antibodies: synergy and antagonism with tumor necrosis factor-α

Murat Cokol, M. Ozturk, T. Yagci, 2012, BMC Cancer.

Novel anti-HER 2 monoclonal antibodies : synergy and antagonism with tumor necrosis factor-α

Murat Cokol, M. Ozturk, T. Yagci, 2012 .