Search Results - Urfali, Mine

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  1. 1
    The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report

    The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlati... by Silan, Fatma, Bourouba, Romyla, Karakaya, Taner, Yildiz, Onur, Paksoy, Baris, Urfali, Mine, Ozdemir, Ozturk

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  2. 2
    Indirect evaluation of amyloid deposition by ultrasonography and its relationship with MEFV gene mutation in FMF patients

    Indirect evaluation of amyloid deposition by ultrasonography and its relationship with MEFV gene mutation in FMF patients by Urfali, Mine, Yilmaz, Gürkan, Özkul, Bahattin, Urfali, Furkan Ertürk

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  3. 3
    Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach?

    Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach? by Sılan, Fatma, Paksoy, Baris, Karakaya, Taner, Yildiz, Onur, Urfali, Mine, Ozdemir, Ozturk

    Published in Biodiscovery
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  4. 4
    The comparison of telomeric DNA length in different biological materials in various cancers by real-time PCR amplification of circulating tumour DNA

    The comparison of telomeric DNA length in different biological materials in various cancers by real-time PCR amplification of circulating tumour DNA by Urfali, Mine, Silan, Fatma, Ozdemir, Ozturk

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  5. 5
    Importance of CYP450 genes rs16947, rs2740574 and rs776746 polymorphisms in colchicine resistance or side effects in FMF patients

    Importance of CYP450 genes rs16947, rs2740574 and rs776746 polymorphisms in colchicine resistance or side effects in FMF patients by Silan, Coskun, Urfali, Mine, Özdemir, Özturk, Silan, Fatma

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  6. 6
    Clinical and molecular characterization of SLC7A gene that located in 14q11.2 locus in a seconder infertile rare case with lysinuric protein intolerance

    Clinical and molecular characterization of SLC7A gene that located in 14q11.2 locus in a seconder infertile rare case with lysinuric protein intolerance by Silan, Fatma, Paksoy, Baris, Urfali, Mine, Karakaya, Taner, Ozdemir, Ozturk

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  7. 7
    The comparison of telomere length in cancer patients: Plasma, whole blood and tumor tissue

    The comparison of telomere length in cancer patients: Plasma, whole blood and tumor tissue by Urfali, Mine, Silan, Fatma, Urfali, Furkan, Gurgen, Atila, Ozdemir, Ozturk

    Published in Medicine science
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  8. 8
    The microdeletion of 15q11.2 locus encompassing TUBGCP5, NIPA1, NIPA2, and CYFIP1 genes in an epileptic case with macrocephaly, attention-deficit/hyperactivity disorder (ADHD), speech and motor delay

    The microdeletion of 15q11.2 locus encompassing TUBGCP5, NIPA1, NIPA2, and CYFIP1 genes in an epileptic case with macrocephaly, attention-deficit/hyperactivity disorder (ADHD), spe... by Ozdemir, Ozturk, Yildiz, Onur, Karakaya, Taner, Paksoy, Baris, Urfali, Mine, Silan, Fatma

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  9. 9
    A mental and motor retarded case with derivative chromosome 8p rearrangements: Genotype–phenotype correlation in a case report

    A mental and motor retarded case with derivative chromosome 8p rearrangements: Genotype–phenotype correlation in a case report by Silan, Fatma, Karakaya, Taner, Yildiz, Onur, Paksoy, Baris, Urfali, Mine, Ozdemir, Ozturk

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  10. 10
    A balanced non-reciprocal translocated case with recurrent abortions: The importance and validity of conventional cytogenetics analysis in balanced translocations detection when comparing to the MicroArray-CGH technique

    A balanced non-reciprocal translocated case with recurrent abortions: The importance and validity of conventional cytogenetics analysis in balanced translocations detection when co... by Ozdemir, Ozturk, Urfali, Mine, Paksoy, Baris, Karakaya, Taner, Yildiz, Onur, Silan, Fatma

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  11. 11
    Alterations in the telomere length distribution of cell-free DNA in human cancer

    Alterations in the telomere length distribution of cell-free DNA in human cancer by Urfali, Mine, Silan, Fatma, Tan, Yusuf Ziya, Celiker, Fatmanur, Guler, Zeliha, Ozdemir, Ozturk

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  12. 12
    The microdeletion/microduplication profiles in spontaneously aborted fetal materials: Double blind results of QF-PCR and MLPA techniques

    The microdeletion/microduplication profiles in spontaneously aborted fetal materials: Double blind results of QF-PCR and MLPA techniques by Silan, Fatma, Ari, Elif, Uludag, Ahmet, Yildiz, Onur, Isin, Betul, Paksoy, Baris, Urfali, Mine, Ozdemir, Ozturk

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  13. 13
    Intercellular Adhesion Molecule-1 K469E and Angiotensinogen T207M Polymorphisms in Coronary Slow Flow

    Intercellular Adhesion Molecule-1 K469E and Angiotensinogen T207M Polymorphisms in Coronary Slow Flow by Gazi, Emine, Barutcu, Ahmet, Altun, Burak, Temiz, Ahmet, Bekler, Adem, Urfali, Mine, Silan, Fatma, Colkesen, Yucel, Ozdemir, Ozturk

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  14. 14
    The morphometry of the cavernous part of the internal carotid artery

    The morphometry of the cavernous part of the internal carotid artery by Farımaz, Mine, Çelik, Hakan Hamdi, Ergun, Kadriye Mine, Akgöz, Ayça, Urfalı, Boran

    Published in Folia morphologica
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