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Page 1
Tetrasomy 12p presenting with long appendix: a prenatal case.
Aydin H, Arisoy R, Geckinli B, Erdogdu E, Karaman A, Gokmeydan E, Pekin O, Tugrul S, Yorganci C. Aydin H, et al. Among authors: karaman a. Genet Couns. 2013;24(4):439-40. Genet Couns. 2013. PMID: 24551989 No abstract available.
The deletion 22q13 syndrome: a new case.
Karaman A, Aydin H, Geçkinli B, Göksu K. Karaman A, et al. Genet Couns. 2015;26(1):53-60. Genet Couns. 2015. PMID: 26043508
Gonadoblastoma in a patient with 46, XY complete gonadal dysgenesis.
Keskin M, Savaş-Erdeve Ş, Kurnaz E, Çetinkaya S, Karaman A, Apaydın S, Aycan Z. Keskin M, et al. Among authors: karaman a. Turk J Pediatr. 2016;58(5):538-540. doi: 10.24953/turkjped.2016.05.013. Turk J Pediatr. 2016. PMID: 28621097 Free article.
AGENESIS OF THE DUCTUS VENOSUS--A CASE WITH NOONAN SYNDROME.
Demirci O, Yavuz T, Arisoy R, Pekin O, Acar H, Aydin H, Cetinkaya A, Karaman A, Erdoğdu E, Kumru P. Demirci O, et al. Among authors: karaman a. Genet Couns. 2015;26(3):373-6. Genet Couns. 2015. PMID: 26625673 No abstract available.
334 results