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Results: 1-6 |
Results: 6

Authors: TOPALOGLU H SEYRANTEPE V KANDEMIR N AKCOREN Z OZGUC M
Citation: H. Topaloglu et al., MTDNA NT3243 MUTATION, EXTERNAL OPHTHALMOPLEGIA, AND HYPOGONADISM IN AN ADOLESCENT GIRL, Pediatric neurology, 18(5), 1998, pp. 429-431

Authors: GUCUYENER K SEYRANTEPE V TOPALOGLU H OZGUC M
Citation: K. Gucuyener et al., MITOCHONDRIAL DELETION IN A BOY WITH GROWTH-HORMONE DEFICIENCY MIMICKING CEREBRAL-PALSY, Journal of inherited metabolic disease, 21(2), 1998, pp. 173-174

Authors: CALI F DIANZANI I DESVIAT LR PEREZ B UGARTE M OZGUC M SEYRANTEPE V SHILOH Y GIANNATTASIO S CARDUCCI C BOSCO P DELEO G PIAZZA A ROMANO V
Citation: F. Cali et al., THE STR252-IVS10NT546-VNTR7 PHENYLALANINE-HYDROXYLASE MINIHAPLOTYPE IN 5 MEDITERRANEAN SAMPLES, Human genetics, 100(3-4), 1997, pp. 350-355

Authors: JOHNS DR DOGULU CF KANSU T SEYRANTEPE V OZGUC M TOPALOGLU H
Citation: Dr. Johns et al., MITOCHONDRIAL-DNA ANALYSIS IN THE TURKISH LHON POPULATION, Neurology, 48(3), 1997, pp. 65007-65007

Authors: SEYRANTEPE V TOPALOGLU H SIMSEK E OZGUC M YORDAM N
Citation: V. Seyrantepe et al., MITOCHONDRIAL-DNA STUDIES IN WOLFRAM (DIDMOAD) SYNDROME, Lancet, 347(9002), 1996, pp. 695-696

Authors: COSKUN T ERKUL E SEYRANTEPE V OZGUC M TOKATLI A OZALP I
Citation: T. Coskun et al., MUTATIONAL ANALYSIS OF TURKISH GALACTOSEMIA PATIENTS, Journal of inherited metabolic disease, 18(3), 1995, pp. 368-369
Risultati: 1-6 |