Yazar "Sezer, Ozlem" için listeleme
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Fibular aplasia, tibial campomelia, and oligosyndactyly: a further patient with a 2-year follow-up
Sezer, Ozlem; Gebesoglu, Ismet; Yuan, Bo; Karaca, Ender; Gokce, Erkan; Gunes, Sezgin (Lippincott Williams & Wilkins, 2014)… -
Trisomy Xq and Xp Deletion Phenotype in a Case with Primary Amenorrhea and Mosaic 45,X/46,X,der(X) Karyotype: Case Report
Kara, Nurten; Okten, Gulsen; Tural, Sengul; Artan, Sevilhan; Sezer, Ozlem; Kocak, Idris (Ortadogu Ad Pres & Publ Co, 2011)The samples of a 18-year-old girl who had a short stature and complaints of hair loss and amenorrhea were sent to our laboratory with a pre-diagnosis of primary amenorrhea. We tried to explain genotype-phenotype relationship ... -
Two turner syndrome patients with the mosaic 45,X/46,X,i(Xq) karyotype: Case report
Gunes, Sezgin; Kara, Nurten; Surucu, Bulent; Okten, Gulsen; Yigit, Serbuelent; Sezer, Ozlem (Ortadogu Ad Pres & Publ Co, 2008)Turner's syndrome is one of the most common chromosomal aneuploidy disorders. Turner's syndrome occurs in 1 in 4000 live-born girls and approximately 5 to 10 percent of them have mosaic isochromosome 45,X/46,X,i(Xq). ...
