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Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|December 17, 2008
The frequency of CYP 21 gene mutations in Turkish women with hyperandrogenismF Kelestimur, H Everest, M Dundar, et al.
Clinical Genetics|June 1, 1997
Polycystic kidney disease, biliary dysgenesis in a patient with Larsen's syndromeS Kurtoglu, M Dundar, I K Hallaç, et al.
The Canadian Journal of Cardiology|March 13, 2009
Lack of association between the Glu298Asp polymorphism of endothelial nitric oxide synthase and slow coronary flow in the Turkish populationA O Caglayan, N Kalay, C Saatci, et al.
Genetic Counseling (Geneva, Switzerland)|November 11, 2008
Can the classical euchromatic variants of 9q12/qh+ cause recurrent abortions?M Dundar, A O Caglayan, C Saatci, et al.
Human Genetics|April 1, 1996
Congenital alacrima in a patient with G (Opitz Frias) syndromeM Dundar, K Erkihç, F Demiryilmaz, et al.
Genetic Counseling (Geneva, Switzerland)|April 28, 2010
A case with a rare chromosomal abnormality: isochromosome 18pM Dundar, A O Caglayan, C Saatci, et al.
Geophysical Research Letters|September 20, 2019
Challenges in the Search for Perchlorate and Other Hydrated Minerals With 2.1-μm Absorptions on MarsE K Leask, B L Ehlmann, M M Dundar, et al.
Genetic Counseling (Geneva, Switzerland)|October 28, 2003
Associated anomalies in asymmetric crying facies and 22q11 deletionM Akcakus, Y Ozkul, T Gunes, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 11, 2000
Patient with Weismann-Netter and Stuhl (toxopachyosteosis) syndrome with communicant hydrocephalus and arachnoid cystS Kurtoglu, M Dundar, S Kumandas, et al.
Genetic Counseling (Geneva, Switzerland)|February 19, 2010
Fluorescence in situ hybridization and single nucleotide polymorphism of a new case with inv dup del(8p)A O Caglayan, J J M Engelen, S Ghesquiere, et al.
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