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1دورية أكاديمية
المؤلفون: Fresko I., Soy M., Hamuryudan V., Yurdakul S., Yavuz Ş., Tümer Z., Yazici H.
المساهمون: Çukurova Üniversitesi
العلاقة: Annals of the Rheumatic Diseases; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://dx.doi.org/10.1136/ard.57.1.45Test; https://hdl.handle.net/20.500.12605/15541Test; 57; 45; 48
الإتاحة: https://doi.org/20.500.12605/15541Test
https://doi.org/10.1136/ard.57.1.45Test
https://hdl.handle.net/20.500.12605/15541Test -
2دورية أكاديمية
المؤلفون: Erdogan, F., Larsen, L.A., Zhang, L., Tuemer, Z., Tommerup, N., Chen, W., Jacobsen, J.R., Schubert, M., Jurkatis, J., Tzschach, A., Ropers, H.H., Ullmann, R.
مصطلحات موضوعية: Technology Platforms
العلاقة: High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease. Erdogan, F. and Larsen, L.A. and Zhang, L. and Tuemer, Z. and Tommerup, N. and Chen, W. and Jacobsen, J.R. and Schubert, M. and Jurkatis, J. and Tzschach, A. and Ropers, H.H. and Ullmann, R. Journal of Medical Genetics 45 (11): 704-709. November 2008
الإتاحة: https://doi.org/10.1136/jmg.2008.058776Test
http://edoc.mdc-berlin.de/10339Test/
https://edoc.mdc-berlin.de/10339Test/ -
3دورية أكاديمية
المؤلفون: Buysse, K., Crepel, A., Menten, B., Pattyn, F., Antonacci, F., A.^Veltman, J., Larsen, L. A., Tümer, Z., de Klein, A., van de Laar, I., Devriendt, K., Mortier, G., Speleman, F.
المصدر: Journal of Medical Genetics; Oct2008, Vol. 45 Issue 10, p672-678, 7p, 1 Chart
مصطلحات موضوعية: GENE mapping, GENETIC techniques, LYMPHOBLASTIC leukemia, POLYMERASE chain reaction, MEDICAL genetics, GENOMICS
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4دورية أكاديمية
المؤلفون: Dlugaszewska, B., Silahtaroglu, A., Menzel, C., Kübart, S., Cohen, M., Mundlos, S., Tümer, Z., Kjaer, K., Friedrich, U., Ropers, H-H., Tommerup, N., Neitzel, H., Kalscheuer, V. M.
المصدر: Journal of Medical Genetics; Feb2006, Vol. 43 Issue 2, p111-118, 8p, 1 Color Photograph, 1 Black and White Photograph, 2 Diagrams
مصطلحات موضوعية: HUMAN chromosome abnormalities, SYNDACTYLY, APERT syndrome, INTELLECTUAL disabilities, ECTOPIC hormones, PURE red cell aplasia, SCOLIOSIS
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5دورية أكاديمية
المصدر: Journal of Medical Genetics; Apr1997, Vol. 34 Issue 4, p265-274, 10p, 1 Color Photograph, 3 Black and White Photographs, 1 Diagram, 2 Charts
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6دورية أكاديمية
المؤلفون: Silahtaroglu, A N, Hacihanefioglu, S, Güven, G S, Cenani, A, Wirth, J, Tommerup, N, Tümer, Z
المصدر: Journal of Medical Genetics; Aug1998, Vol. 35 Issue 8, p682-684, 3p
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7دورية أكاديمية
المؤلفون: Tümer, Z, Tønnesen, T, Böhmann, J, Marg, W, Horn, N
المصدر: Journal of Medical Genetics; Aug1994, Vol. 31 Issue 8, p615-617, 3p, 1 Diagram, 1 Graph
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8دورية أكاديمية
المؤلفون: Tommerup, N, Tümer, Z, Tønnesen, T, Horn, N
المصدر: Journal of Medical Genetics; Apr1993, Vol. 30 Issue 4, p314-315, 2p