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Page 1
657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish population.
Hum Biol. 2005 Jun;77(3):393-7. doi: 10.1353/hub.2005.0056.
Hum Biol. 2005.
PMID: 16392640
Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey.
Tekin M, Akçayöz D, Comak E, Boğoçlu G, Duman T, Fitoz S, Ilhan I, Akar N.
Tekin M, et al. Among authors: akcayoz d.
Clin Genet. 2003 Oct;64(4):371-4. doi: 10.1034/j.1399-0004.2003.00144.x.
Clin Genet. 2003.
PMID: 12974744
No abstract available.
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Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome.
Ergür AT, Ocal G, Berberoglu M, Tekin M, Kiliç BG, Aycan Z, Kutlu A, Adiyaman P, Siklar Z, Akar N, Sahin A, Akçayöz D.
Ergür AT, et al. Among authors: akcayoz d.
Pediatr Int. 2008 Apr;50(2):172-4. doi: 10.1111/j.1442-200X.2008.02540.x.
Pediatr Int. 2008.
PMID: 18353053
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A novel missense mutation in a C2 domain of OTOF results in autosomal recessive auditory neuropathy.
Tekin M, Akcayoz D, Incesulu A.
Tekin M, et al. Among authors: akcayoz d.
Am J Med Genet A. 2005 Sep 15;138(1):6-10. doi: 10.1002/ajmg.a.30907.
Am J Med Genet A. 2005.
PMID: 16097006
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