Showing 101 - 120 results of 444 for search '"Balkan Journal of Medical Genetics"', query time: 0.56s Refine Results
  1. 101
    Molecular Characterization of Microrna Interference and Aristolochic Acid Intoxication Found in Upper Tract Urothelial Carcinoma in Patients with Balkan Endemic Nephropathy: A Systematic Review of the Current Literature

    Molecular Characterization of Microrna Interference and Aristolochic Acid Intoxication Found in Upper Tract Urothelial Carcinoma in Patients with Balkan Endemic Nephropathy: A Syst... by Bašić D, Ignjatović I, Janković Veličković Lj, Veljković A

    Published 2022-12-01
    “…Balkan Journal of Medical Genetics…”
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  2. 102
    Having Multiple Renal Cysts in a Young Adult is Not Always a Sign of Polycystic Kidney Disease

    Having Multiple Renal Cysts in a Young Adult is Not Always a Sign of Polycystic Kidney Disease by Kaynar K, Kayıpmaz S, Çebi AH, Hüseynova Ş

    Published 2022-06-01
    “…Balkan Journal of Medical Genetics…”
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  3. 103
    Prevalence of Chromosomal Abnormalities in Infertile Couples in Romania

    Prevalence of Chromosomal Abnormalities in Infertile Couples in Romania by Mierla Dana, Malageanu M., Tulin R., Albu D.

    Published 2015-06-01
    “…Balkan Journal of Medical Genetics…”
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  4. 104
    Matrix metalloproteinase-2 (MMP-2 ) and-9 (MMP-9) gene variants and microvascular complications in type 2 diabetes patients

    Matrix metalloproteinase-2 (MMP-2 ) and-9 (MMP-9) gene variants and microvascular complications in type 2 diabetes patients by Andjelic Jelic M, Radojkovic D, Nikolic A, Rakicevic Lj, Babic T, Jelic D, Lalic NM

    Published 2023-03-01
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  5. 105
    Prenatal diagnosis of organic acidemias at a tertiary center

    Prenatal diagnosis of organic acidemias at a tertiary center by Tanacan A, Gurbuz BB, Aydin E, Erden M, Coskun T, Beksac MS

    Published 2019-08-01
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  6. 106
    Determining specific thyroid transcripts in peripheral blood: A single center study experience

    Determining specific thyroid transcripts in peripheral blood: A single center study experience by Makazlieva T, Eftimov A, Vaskova O, Tripunoski T, Miladinova D, Risteski S, Jovanovic H, Jakovski Z

    Published 2018-12-01
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  7. 107
    Duplication of the SOX3 gene in an sry-negative 46,XX male with associated congenital anomalies of kidneys and the urinary tract: Case report and review of the literature

    Duplication of the SOX3 gene in an sry-negative 46,XX male with associated congenital anomalies of kidneys and the urinary tract: Case report and review of the literature by Tasic V, Mitrotti A, Riepe FG, Kulle AE, Laban N, Polenakovic M, Plaseska-Karanfilska D, Sanna-Cherchi S, Kostovski M, Gucev Z

    Published 2019-08-01
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  8. 108
    Investigation of the N-terminal coding region of MUC7 alterations in dentistry students with and without caries

    Investigation of the N-terminal coding region of MUC7 alterations in dentistry students with and without caries by Koç Öztürk L, Yarat A, Akyuz S, Furuncuoglu H, Ulucan K

    Published 2016-06-01
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  9. 109
    Detection of the GJB2 Mutation in Iranian Children with Hearing Loss Treated with Cochlear Implantation

    Detection of the GJB2 Mutation in Iranian Children with Hearing Loss Treated with Cochlear Implantation by Peyvandi A, Morovvati S, Rabiee H, Ranjbar R, Ajalloueyan M, Hassanalifard M

    Published 2011-01-01
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  10. 110
    Human Leukocyte Antigen-B27 and Disease Susceptibility in Vojvodina, Serbia

    Human Leukocyte Antigen-B27 and Disease Susceptibility in Vojvodina, Serbia by Vojvodić S., Ademović-Sazdanić D., Busarčević I.

    Published 2012-12-01
    “…Balkan Journal of Medical Genetics…”
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  11. 111
    PCSK9 gene participates in the development of primary dyslipidemias

    PCSK9 gene participates in the development of primary dyslipidemias by Matías-Pérez D, Pérez-Santiago AD, Sánchez Medina MA, Alpuche Osorno JJ, García-Montalvo IA

    Published 2021-07-01
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  12. 112
    Aplasia Ras Homologous Member I Gene and Development of Glial Tumors

    Aplasia Ras Homologous Member I Gene and Development of Glial Tumors by Yakut S, Tuncer M, Berker M, Goksu E, Gurer I, Ozes O, Luleci G, Karauzum S

    Published 2011-01-01
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  13. 113
    Forensic Value of Ten Short Tandem Repeat Loci in Turkey Compared to Other Ethnic Groups

    Forensic Value of Ten Short Tandem Repeat Loci in Turkey Compared to Other Ethnic Groups by Ozkorkmaz A, Baransel Isir A, Pehlivan S, Özkorkmaz E

    Published 2009-01-01
    “…Balkan Journal of Medical Genetics…”
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  14. 114
    RANKL is a new epigenetic biomarker for the vasomotor symptom during Menopause

    RANKL is a new epigenetic biomarker for the vasomotor symptom during Menopause by Kalkan R, Altarda M, Tosun O

    Published 2020-08-01
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  15. 115
    Ankyloblepharon-ectodermal defects-cleft lip-palate syndrome due to a novel missense mutation in the SAM domain of the TP63 gene

    Ankyloblepharon-ectodermal defects-cleft lip-palate syndrome due to a novel missense mutation in the SAM domain of the TP63 gene by Tajir M, Lyahyai J, Guaoua S, El Alloussi M, Sefiani A

    Published 2020-08-01
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  16. 116
    Vitamin D receptor polymorphisms among the Turkish population are associated with multiple sclerosis

    Vitamin D receptor polymorphisms among the Turkish population are associated with multiple sclerosis by Bulan B, Hoscan AY, Keskin SN, Cavus A, Culcu EA, Isik N, List EO, Arman A

    Published 2023-03-01
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  17. 117
    Dual effect of the GHRL gene variant in the molecular pathogenesis of obesity

    Dual effect of the GHRL gene variant in the molecular pathogenesis of obesity by Becer E, Ergoren MC

    Published 2021-07-01
    “…Balkan Journal of Medical Genetics…”
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  18. 118
    Phenotypic Variability of Cowden Syndrome Within a Single Family: Impact on Diagnosis, Management and Genetic Counselling

    Phenotypic Variability of Cowden Syndrome Within a Single Family: Impact on Diagnosis, Management and Genetic Counselling by Ilic N, Mitrovic N, Radeta R, Krasić S, Vukomanović V, Samardzija G, Vasic M, Vlahovic A, Sarajlija A

    Published 2025-03-01
    “…Balkan Journal of Medical Genetics…”
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  19. 119
    Features of the Wolf-Hirschhorn Syndrome (WHS) from Infant to Young Teenager

    Features of the Wolf-Hirschhorn Syndrome (WHS) from Infant to Young Teenager by Popescu D.E., Marian D., Zeleniuc M., Samoila Ch., Belengeanu V.

    Published 2023-07-01
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  20. 120
    Three Novel Mutations of CHD7 Gene in Two Turkish Patients with Charge Syndrome; A Double Point Mutation and an Insertion

    Three Novel Mutations of CHD7 Gene in Two Turkish Patients with Charge Syndrome; A Double Point Mutation and an Insertion by Giray Bozkaya Ozlem, Ataman E., Randa C., Onur Cura D., Gürsoy S., Aksel O., Ulgenalp A.

    Published 2015-06-01
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