المؤلفون: Ozdemir O., Silan F., Urfali U., Uludag A., Ari E., Kayatas M.

المساهمون: Ozdemir, O., Cumhuriyet University, Faculty of Medicine, Department of Medical Genetics, 58140, Sivas, Turkey, Canakkale Onsekiz Mart University, Faculty of Medicine, Department of Medical Genetics, 17100, Canakkale, Turkey -- Silan, F., Canakkale Onsekiz Mart University, Faculty of Medicine, Department of Medical Genetics, 17100, Canakkale, Turkey -- Urfali, U., Canakkale Onsekiz Mart University, Faculty of Medicine, Department of Medical Genetics, 17100, Canakkale, Turkey -- Uludag, A., Cumhuriyet University, Faculty of Medicine, Department of Medical Genetics, 58140, Sivas, Turkey -- Ari, E., Cumhuriyet University, Faculty of Medicine, Department of Medical Genetics, 58140, Sivas, Turkey -- Kayatas, M., Cumhuriyet University, Faculty of Medicine, Department of Nephrology, 58140, Sivas, Turkey

مصطلحات موضوعية: R.Msp1 fragmentation, Chronic renal failure, DNA hypomethylation, SNP, Epigenetics, MTHFR C677T

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3104::f6d208f07c626c61d3751f382da9125a
https://hdl.handle.net/20.500.12418/5467

المؤلفون: Becker, K, Clayton-Smith, J, Borozdin, W, Boehm, D, Lehipoldt, M, Wilhelm, C, Reardon, W, Winter, R, Muhlendyck, H, Giray Bozkaya, Özlem, Kohlhase, J, Silan, F

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2605::fee44165d44aa4c0025f3848e9fc1f14
https://avesis.deu.edu.tr/publication/details/00153579-4b4b-4d77-8d5b-5de08987e69c/oai

المؤلفون: Bak, M., Fonseca, A., Mehrjouy, M., Rasmussen, M., Halgren, C., Bache, I., Kroisel, P., Midyan, S., Vermeesch, J., Vienna-Morgante, A., Abe, K., Moretti-Ferreira, D., Angelova, L., Rajcan-Separovic, E., Sismani, C., Aristidou, C., Sedlacek, Z., Fagerberg, C., Brondum-Nielsen, K., Vogel, I., Bojesen, A., Ounap, K., Roht, L., Lespinasse, J., Beneteau, C., Kalscheuer, V., Ehmke, N., Daumer-Haas, C., Stefanou, E., Czako, M., Sheth, F., Bonaglia, C., Novelli, A., Fannemel, M., Engelen, J., Travessa, A., Kokalj-Vokac, N., Ramos-Arroyo, M., Martinez, L. R., Guitart, M., Schinzel, A., Silan, F., de Almeida, C., Akkari, Y., Batanian, J., Kim, H., Jacky, P., Tommerup, N., Consortium, Int Breakpoint Mapping

المصدر: Bak, M, Fonseca, A, Mehrjouy, M, Rasmussen, M, Halgren, C, Bache, I, Kroisel, P, Midyan, S, Vermeesch, J, Vienna-Morgante, A, Abe, K, Moretti-Ferreira, D, Angelova, L, Rajcan-Separovic, E, Sismani, C, Aristidou, C, Sedlacek, Z, Fagerberg, C, Brondum-Nielsen, K, Vogel, I, Bojesen, A, Ounap, K, Roht, L, Lespinasse, J, Beneteau, C, Kalscheuer, V, Ehmke, N, Daumer-Haas, C, Stefanou, E, Czako, M, Sheth, F, Bonaglia, C, Novelli, A, Fannemel, M, Engelen, J, Travessa, A, Kokalj-Vokac, N, Ramos-Arroyo, M, Martinez, L R, Guitart, M, Schinzel, A, Silan, F, de Almeida, C, Akkari, Y, Batanian, J, Kim, H, Jacky, P, Tommerup, N & Consortium, I B M 2019, ' Morbidity risk of chromosomal breakpoints in topological domains enriched in non-exonic conserved elements ', European Journal of Human Genetics, vol. 26, pp. 59-60 . https://doi.org/10.1038/s41431-018-0249-5

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3062::075fd0f2c1e5697e2c033e24afc94e89
https://portal.findresearcher.sdu.dk/da/publications/e71d9f5a-8f73-405f-a9e4-7047bea99997

المؤلفون: Gulec Balbay, E., Küçük, E., Balbay, O., Ali Nihat Annakkaya, Silan, F., Meliha Hiz, M.

المصدر: Scopus-Elsevier

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0ae185e8dcd735f827cf9d79058e0101
http://www.scopus.com/inward/record.url?eid=2-s2.0-84899109971&partnerID=MN8TOARS

المؤلفون: Silan F, Aydogan I, Kavak A, Bardaro T, D'Urso M

المصدر: International journal of dermatology 43 (2004): 527–529.
info:cnr-pdr/source/autori:Silan F, Aydogan I, Kavak A, Bardaro T, D'Urso M/titolo:Incontinentia pigmenti with NEMO mutation in a Turkish family/doi:/rivista:International journal of dermatology/anno:2004/pagina_da:527/pagina_a:529/intervallo_pagine:527–529/volume:43

URL الوصول: https://explore.openaire.eu/search/publication?articleId=cnr_________::50ea3712e0ed505e063482a633d9fdf0
http://www.cnr.it/prodotto/i/26878

المؤلفون: Ribero, S., Osella Abate, S., Pasquali, S., Rossi, C.R., Borgognoni, L., Piazzalunga, D., Solari, N., Schiavon, M., Brandani, P., Ansaloni, L., Ponte, E., Silan, F., Sommariva, A., Bellucci, F., Macripò, G., Quaglino, P., On Behalf Of The Italian Melanoma Intergroup (IMI)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::811e06b29ecd56f0ffc39caf04a1231a

المؤلفون: Battal F, Silan F, Topaloğlu N, Aylanç H, Yıldırım Ş, Köksal Binnetoğlu F, Tekin M, Kaymaz N, Ozdemir O

المصدر: Balkan Journal of Medical Genetics, Vol 19, Iss 2, Pp 23-28 (2016)

مصطلحات موضوعية: amyloidosis, children, familial mediterranean fever (fmf), genotype-phenotype correlations, pathogenic variant, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1311-0160

URL الوصول: https://doaj.org/article/e462c4ab4da84feca36ccf07c2012539

المؤلفون: Uludağ A, Uysal A, Ertekin YH, Tekin M, Kütük B, Silan F, Özdemir Ö

المصدر: Balkan Journal of Medical Genetics, Vol 19, Iss 1, Pp 29-34 (2016)

مصطلحات موضوعية: abnormal hemoglobin (hb), β-thalassemia (β-thal), premarital screening, prevalence, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1311-0160

URL الوصول: https://doaj.org/article/a8fc542be888445aac8f90d7318521cd

المؤلفون: Sen H. M., Silan F., Degirmenci Y., Kamaran Ozisik H. I.

المصدر: Balkan Journal of Medical Genetics, Vol 17, Iss 2, Pp 37-41 (2014)

مصطلحات موضوعية: ischemic cerebrovascular disease (icvd), clopidogrel, cyp2c19 and p2y12 gene polymorphisms, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1311-0160

URL الوصول: https://doaj.org/article/fafea0486724460cb918538fe68b1c4e

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