المؤلفون: Ikbal Atli E, Gurkan H, Onur Kirkizlar H, Atli E, Demir S, Yalcintepe S, Kalkan R, Demir AM

المصدر: Balkan Journal of Medical Genetics, Vol 23, Iss 2, Pp 59-64 (2021)

مصطلحات موضوعية: cytogenetics, fluorescent in situ hybridization (fish), multiple myeloma, next generation sequencing (ngs), Genetics, QH426-470

وصف الملف: electronic resource

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

URL الوصول: https://doaj.org/article/c43383aad31647ac81898551345cca6b

المؤلفون: Mitani T, Isikay S, Gezdirici A, Gulec EY, Punetha J, Fatih JM, Herman I, Akay G, Du H, Calame DG, Ayaz A, Tos T, Yesil G, Aydin H, Geckinli B, Elcioglu N, Candan S, Sezer O, Erdem HB, Gul D, Demiral E, Elmas M, Yesilbas O, Kilic B, Gungor S, Ceylan AC, Bozdogan S, Ozalp O, Cicek S, Aslan H, Yalcintepe S, Topcu V, Bayram Y, Grochowski CM, Jolly A, Dawood M, Duan R, Jhangiani SN, Doddapaneni H, Hu J, Muzny DM, Baylor-Hopkins Center for Mendelian Genomics, Marafi D, Akdemir ZC, Karaca E, Carvalho CMB, Gibbs RA, Posey JE, Lupski JR, Pehlivan D.

Relation: Am J Hum Genet; https://hdl.handle.net/20.500.12645/37689

الاتاحة: https://hdl.handle.net/20.500.12645/37689
https://doi.org/10.1016/j.ajhg.2021.08.009

المؤلفون: Yalcintepe S., Maras T., Kizilyar I., SezginerGuler H., Zhuri D., Atli E., Ozen Y., Gurkan H.

مصطلحات موضوعية: Medicine, Canavan disease, ASPA, Loss of heterozygosity

Relation: https://figshare.com/articles/dataset/Supplementary_Material_for_Homozygous_Paternally_Inherited_i_ASPA_i_Variant_in_a_Patient_with_Canavan_Disease/25233682

الاتاحة: https://doi.org/10.6084/m9.figshare.25233682.v1

المؤلفون: Gürkan, H., Atlı, E., Yalçıntepe, S., Demir, S., Özen, Y., Tozkır, Hilmi

Relation: European Journal Of Human Genetics; Konferans Öğesi - Uluslararası - Kurum Öğretim Elemanı; https://hdl.handle.net/20.500.11776/4912; 28; SUPPL 1; 909; WOS:000598482603233

الاتاحة: https://hdl.handle.net/20.500.11776/4912

المؤلفون: Atli E.I. (11839178), Yalcintepe S. (11839181), Atli E. (11839184), Demir S. (11839187), Mail C. (11839190), Gurkan H. (11839193)

مصطلحات موضوعية: Medicine, Array CGH, Clinical heterogeneity, Copy number variation, Microdeletion syndrome, Microduplication syndrome, Molecular cytogenetics

Relation: https://figshare.com/articles/dataset/Supplementary_Material_for_Clinical_Implications_of_Chromosome_16_Copy_Number_Variation/17205773

الاتاحة: https://doi.org/10.6084/m9.figshare.17205773.v1

المؤلفون: Sarikaya Solak, S., Yalcıntepe, S., Atahan, C., Nagy, N., Can, N.

المصدر: Clinical and Experimental Dermatology ; volume 45, issue 4, page 508-511 ; ISSN 0307-6938 1365-2230

مصطلحات موضوعية: Dermatology

الاتاحة: http://dx.doi.org/10.1111/ced.14144
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fced.14144
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ced.14144
https://onlinelibrary.wiley.com/doi/full-xml/10.1111/ced.14144

المؤلفون: Ikbal Atli, E, Gurkan, H, Onur Kirkizlar, H, Atli, E, Demir, S, Yalcintepe, S, Kalkan, R, Demir, AM

المصدر: Balkan Journal of Medical Genetics; 2020, Vol. 23 Issue 2, p59-64, 6p

مصطلحات موضوعية: FLUORESCENCE in situ hybridization, MULTIPLE myeloma, DIAGNOSIS, BONE marrow cells, PLASMACYTOMA, PLASMA cells, IN situ hybridization, KARYOTYPES

المؤلفون: Ikbal Atli, E, Gurkan, H, Onur Kirkizlar, H, Atli, E, Demir, S, Yalcintepe, S, Kalkan, R, Demir, AM

المصدر: Balkan Journal of Medical Genetics; March 2021, Vol. 23 Issue: 2 p59-64, 6p