| Cytogenetic analysis of 4216 patients referred for suspected chromosomal abnormalities in Southeast Turkey M Balkan, H Akbas, H Isi, D Oral, A Turkyilmaz, S Kalkanli, S Simsek, ... Genet Mol Res 9 (2), 1094-103, 2010 | 95 | 2010 |
| The insertion/deletion polymorphism in the ACE gene and chronic obstructive pulmonary disease S Simsek, S Tekes, D Oral, A Turkyilmaz, B Isik, MR Isik, H Akkoc Genet Mol Res 12 (2), 1392-1398, 2013 | 35 | 2013 |
| Angiotensin-converting enzyme gene insertion/deletion polymorphism with metabolic syndrome in Turkish patients S Simsek, S Tekes, A Turkyilmaz, AK Tuzcu, F Kılıc, NN Culcu, B Isık, ... Journal of Endocrinological Investigation 36, 860-863, 2013 | 11 | 2013 |
| Prenatal diagnosis of 4p and 4q subtelomeric microdeletion in de novo ring chromosome 4 H Akbas, N Cine, M Erdemoglu, AE Atay, S Simsek, A Turkyilmaz, ... Case Reports in Obstetrics and Gynecology 2013, 2013 | 6 | 2013 |
| Genetic analysis in pregnancy with fetal pathologic ultrasound findings S Simsek, A Turkyilmaz, D Oral, A Yalinkaya, S Tekes, H Akbas, T Budak Biotechnology & Biotechnological Equipment 27 (3), 3829-3833, 2013 | 2 | 2013 |
| Genetics analysis with down syndrome and histopathological examination of buccal epithelial cells S Kalkanli, S Simsek, M Balkan, H Akbas, H Isi, D Oral, A Turkyılmaz, ... Int. j. morphol 31 (2), 668-671, 2013 | 1 | 2013 |
| Evaluation of etiologic causes of recurrent pregnancy loss M Obut, MS EVSEN, HE Soydinç, ME Sak, A OZLER, M Fidanboy, ... Journal of Turkish Society of Obstetrics and Gynecology 10 (2), 67-71, 2013 | 1 | 2013 |
| A de novo reciprocal t (1; 17) translocation with regular trisomy 21 S Simsek, A Turkyilmaz, ISI Hilmi, O Diclehan, S Tekes, MN Talay International Archives of Medical Research 4 (2), 15-18, 2012 | 1 | 2012 |
| Cystathionine synthase T833C/844ins68 Polymorphism: A family-based study on down syndromes children A TURKYILMAZ, S SIMSEK, O Diclehan, S TEKEŞ, ISI Hilmi International Archives of Medical Research 2 (2), 54-56, 2011 | 1 | 2011 |
| Study about 4p and 4q Subtelomeric Microdeletion in De Novo Ring Chromosome 4 H Akbas, M Erdemoflu, AE Atay, S Simsek, M Balkan, A Turkyilmaz, ... BP International, 2022 | | 2022 |
| Análisis Genético y Examen Histopatológico de las Células Epiteliales Bucales en pacientes con Síndrome de Down S Kalkanli, S Simsek, M Balkan, H Akbas, H Isi, D Oral, A Turkyilmaz, ... International Journal of Morphology 31 (2), 668-671, 2013 | | 2013 |
| Case Report Prenatal Diagnosis of 4p and 4q Subtelomeric Microdeletion in De Novo Ring Chromosome 4 H Akbas, N Cine, M Erdemoglu, AE Atay, S Simsek, A Turkyilmaz, ... | | 2013 |
| The outcomes of prenatal karyotype analysis in amniocentesis and fetal blood sampling S SIMSEK, A TURKYILMAZ, O Diclehan, A YALINKAYA, S TEKES, ... International Archives of Medical Research 2 (2), 57-59, 2011 | | 2011 |
| A Middle Aged Woman with Mosaic Turner Syndrome: A Case Report S Simsek, A Yalinkaya, D Oral, A Turkyilmaz, S Tekes, T Budak Journal Of International Dental And Medical Research 4 (2), 100-103, 2011 | | 2011 |
| Female Pseudohermaphroditism In A 68 Year Old Patient: A Case Report S Sımsek, A Turkyılmaz, H Isı, D Oral, S Tekes, A Yalınkaya International Archives of Medical Research 3 (1), 23-27, 2011 | | 2011 |
| RECURRENT MISCARRIAGES IN A COUPLE WITH T (4, 8) AND INV (9) D Oral, S Kalkanli-Tas, M Fidanboy, A Turkyilmaz, T Budak IUBMB LIFE 61 (3), 357-357, 2009 | | 2009 |
| PRENATAL DIAGNOSTIC RESULTS OF 241 CASES WITH HIGH RISK IN SCREENING TESTS S Simsek, A Turkyilmaz, H Akbas, S Tekes, M Balkan, T Budak IUBMB LIFE 61 (3), 374-374, 2009 | | 2009 |
| A RARE CASE MOSAIC 16 A Turkyilmaz, D Oral, H Isi, M Balkan IUBMB LIFE 61 (3), 350-350, 2009 | | 2009 |
| AN AZOOSPERMIC CASE WITH Y ISOCHROMOSOME A Turkyilmaz, D Oral, S Simsek, H Isi IUBMB LIFE 61 (3), 329-329, 2009 | | 2009 |
| TURNER-DOWN SYNDROME: A CASE REPORT D Oral, S Simsek, A Turkyilmaz, M Balkan IUBMB LIFE 61 (3), 335-335, 2009 | | 2009 |
