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Page 1
Two novel mutations in XYLT2 cause spondyloocular syndrome.
Taylan F, Yavaş Abalı Z, Jäntti N, Güneş N, Darendeliler F, Baş F, Poyrazoğlu Ş, Tamçelik N, Tüysüz B, Mäkitie O. Taylan F, et al. Among authors: bas f. Am J Med Genet A. 2017 Dec;173(12):3195-3200. doi: 10.1002/ajmg.a.38470. Epub 2017 Sep 8. Am J Med Genet A. 2017. PMID: 28884924
Thyroid ultrasound in IDDM.
Darendeliler FF, Kadioğlu A, Bas F, Bundak R, Günöz H, Saka N, Neyzi OR. Darendeliler FF, et al. Among authors: bas f. J Pediatr Endocrinol. 1994 Jan-Mar;7(1):33-7. doi: 10.1515/jpem.1994.7.1.33. J Pediatr Endocrinol. 1994. PMID: 7910507
Spironolactone therapy in hypertrichosis.
Darendeliler F, Bas F, Balaban S, Bundak R, Demirkol D, Saka N, Gunoz H. Darendeliler F, et al. Among authors: bas f. Eur J Endocrinol. 1996 Nov;135(5):604-8. doi: 10.1530/eje.0.1350604. Eur J Endocrinol. 1996. PMID: 8980164 Clinical Trial.
Brachymetacarpia V in familial short stature.
Sükür M, Darendeliler F, Bundak R, Baş F, Saka N, Günöz H. Sükür M, et al. Among authors: bas f. Ann Hum Biol. 1997 Jul-Aug;24(4):371-5. doi: 10.1080/03014469700005122. Ann Hum Biol. 1997. PMID: 9239443 Free article.
215 results