المؤلفون: Plaseska-Karanfilska Dijana, Atanasovska B, Bozhinovski G, Chakalova L, Kocheva S, Karanfilski O

المصدر: Balkan Journal of Medical Genetics, Vol 15, Iss Supplement, Pp 61-65 (2012)

مصطلحات موضوعية: hb lepore, hemoglobinopathy, molecular diagnostics, thalassemia., Genetics, QH426-470

وصف الملف: electronic resource

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

URL الوصول: https://doaj.org/article/1aa4a8252d9245bd9c8ee20f0d57db70

المؤلفون: Plaseska-Karanfilska Dijana, Sukarova-Stefanovska E, Kocheva S, Maleva I, Noveski P, Kiprijanovska S, Stankova K, Dimcev P, Madjunkov M, Madjunkova S

المصدر: Balkan Journal of Medical Genetics, Vol 15, Iss Supplement, Pp 39-43 (2012)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

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

URL الوصول: https://doaj.org/article/0f0edd8ebc9744a392b999e5d64cdef1

المؤلفون: Kocheva S, Trivodalieva S, Vlaski-Jekic S, Kuturec M, Efremov G

المصدر: Balkan Journal of Medical Genetics, Vol 11, Iss 1, Pp 61-64 (2008)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

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

URL الوصول: https://doaj.org/article/b01e4f5dcb9c4520b3268bde66c1a07e

المؤلفون: Kocheva S, Trivodalieva S, Plaseska-Karanfilska D, Vlaski-Jekic S, Kuturec M, Efremov G

المصدر: Balkan Journal of Medical Genetics, Vol 11, Iss 2, Pp 59-63 (2008)

مصطلحات موضوعية: duchenne muscular dystrophy (dmd), multiplex polymerase chain reaction (mpcr), multiplex ligation-dependent probe amplification (mlpa), short tandem repeat (str), Genetics, QH426-470

وصف الملف: electronic resource

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

URL الوصول: https://doaj.org/article/d4c78be396c74c93b660aff11a90e23c

المؤلفون: Kocheva S, Vlaski-Jekic S, Kuturec M, Efremov G

المصدر: Balkan Journal of Medical Genetics, Vol 10, Iss 2, Pp 55-60 (2007)

مصطلحات موضوعية: spinal muscular atrophy (sma), survival motor neuron (smn) gene, neuronal apoptosis inhibitory protein (naip) gene, Genetics, QH426-470

وصف الملف: electronic resource

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

URL الوصول: https://doaj.org/article/5e2f86530c0244e88729e5fd49ecd302

المؤلفون: Martinova, K, Coneska-Jovanova, B, Kocheva, S, Jovanovska, A, Bojadgieva, E

المصدر: Archives of Disease in Childhood ; volume 99, issue Suppl 2, page A300.1-A300 ; ISSN 0003-9888 1468-2044

الاتاحة: http://dx.doi.org/10.1136/archdischild-2014-307384.823
https://syndication.highwire.org/content/doi/10.1136/archdischild-2014-307384.823

المؤلفون: Martinova, K, Coneska-Jovanova, B, Kocheva, S, Jovanovska, A, Bojadgieva, E

المصدر: Archives of Disease in Childhood ; volume 99, issue Suppl 2, page A299.3-A300 ; ISSN 0003-9888 1468-2044

الاتاحة: http://dx.doi.org/10.1136/archdischild-2014-307384.822
https://syndication.highwire.org/content/doi/10.1136/archdischild-2014-307384.822

المؤلفون: Dork T., Macek M., Mekus F., Tummler B., Tzountzouris J., Casals T., Krebsova A., Koudova M., Sakmaryova I., Vavrova V., Zemkova D., Ginter E., Petrova N. V., Ivaschenko T., Baranov V., Witt M., Pogorzelski A., Bal J., Zekanowsky C., Wagner K., Stuhrmann M., Bauer I., Seydewitz H. H., Neumann T., Jakubiczka S., Kraus C., Thamm B., Nechiporenko M., Livshits L., Mosse N., Tsukerman G., Kadasi L., Ravnik-Glavac M., Glavac D., Komel R., Vouk K., Kucinskas V., Krumina A., Teder M., Kocheva S., Efremov G. D., Onay T., Kirdar B., Malone G., Schwarz M., Zhou Z., Friedman K. J., Carles S., Claustres M., Bozon D., Verlingue C., Ferec C., Tzetis M., Kanavakis E., Cuppens H., Bombieri C., Pignatti P. F., Sangiuolo F., Jordanova A., Kusic J., Radojkovic D., Sertic J., Richter D., Rukavina A. S., Bjorck E., Strandvik B., Cardoso H., Montgomery M., Nakielna B., Hughes D., Estivill X., Aznarez I., Tullis E., Tsui L. -C., Zielenski J.

المساهمون: Dork, T., Macek, M., Mekus, F., Tummler, B., Tzountzouris, J., Casals, T., Krebsova, A., Koudova, M., Sakmaryova, I., Vavrova, V., Zemkova, D., Ginter, E., Petrova, N. V., Ivaschenko, T., Baranov, V., Witt, M., Pogorzelski, A., Bal, J., Zekanowsky, C., Wagner, K., Stuhrmann, M., Bauer, I., Seydewitz, H. H., Neumann, T., Jakubiczka, S., Kraus, C., Thamm, B., Nechiporenko, M., Livshits, L., Mosse, N., Tsukerman, G., Kadasi, L., Ravnik-Glavac, M., Glavac, D., Komel, R., Vouk, K., Kucinskas, V., Krumina, A., Teder, M., Kocheva, S., Efremov, G. D., Onay, T., Kirdar, B., Malone, G., Schwarz, M., Zhou, Z., Friedman, K. J., Carles, S., Claustres, M., Bozon, D., Verlingue, C., Ferec, C., Tzetis, M., Kanavakis, E., Cuppens, H., Bombieri, C., Pignatti, P. F., Sangiuolo, F., Jordanova, A., Kusic, J., Radojkovic, D., Sertic, J., Richter, D., Rukavina, A. S., Bjorck, E., Strandvik, B., Cardoso, H., Montgomery, M., Nakielna, B., Hughes, D., Estivill, X., Aznarez, I., Tullis, E., Tsui, L. -C., Zielenski, J.

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/10798353; info:eu-repo/semantics/altIdentifier/wos/WOS:000086661100001; volume:106; issue:3; firstpage:259; lastpage:268; numberofpages:10; journal:HUMAN GENETICS; http://hdl.handle.net/11562/225499; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0342657015

الاتاحة: http://hdl.handle.net/11562/225499
https://doi.org/10.1007/s004390000246

المؤلفون: By:dork, T, Macek, M, Mekus, F, Tummler, B, Tzountzouris, J, Casals, T, Krebsova, A, Koudova, M, Sakmaryova, I, Vavrova, V, Zemkova, D, Ginter, E, Petrova, N, Ivaschenko, T, Baranov, V, Witt, M, Pogorzelski, A, Bal, J, Zekanowsky, C, Wagner, K, Stuhrmann, M, Bauer, I, Seydewitz, H, Neumann, T, Jakubiczka, S, Kraus, C, Thamm, B, Nechiporenko, M, Livshits, L, Mosse, N, Tsukerman, G, Kadasi, L, Ravnik Glavac, M, Glavac, D, Komel, R, Vouk, K, Kucinskas, V, Krumina, A, Teder, M, Kocheva, S, Efremov, G, Onay, T, Kirdar, B, Malone, G, Schwarz, M, Zhou, Z, Friedman, K, Carles, S, Claustres, M, Bozon, D, Verlingue, C, Ferec, C, Tzetis, M, Kanavakis, E, Cuppens, H, Bombieri, C, Pignatti, P, Jordanova, A, Kusic, J, Radojkovic, D, Sertic, J, Richter, D, Rukavina, A, Bjorck, E, Strandvik, B, Cardoso, H, Montgomery, M, Nakielna, B, Hughes, D, Estivill, X, Aznarez, I, Tullis, E, Tsui, L, Zielenski, Jl, SANGIUOLO, FEDERICA CARLA

المساهمون: By:dork, T, Macek, M, Mekus, F, Tummler, B, Tzountzouris, J, Casals, T, Krebsova, A, Koudova, M, Sakmaryova, I, Vavrova, V, Zemkova, D, Ginter, E, Petrova, N, Ivaschenko, T, Baranov, V, Witt, M, Pogorzelski, A, Bal, J, Zekanowsky, C, Wagner, K, Stuhrmann, M, Bauer, I, Seydewitz, H, Neumann, T, Jakubiczka, S, Kraus, C, Thamm, B, Nechiporenko, M, Livshits, L, Mosse, N, Tsukerman, G, Kadasi, L, Ravnik Glavac, M, Glavac, D, Komel, R, Vouk, K, Kucinskas, V, Krumina, A, Teder, M, Kocheva, S, Efremov, G, Onay, T, Kirdar, B, Malone, G, Schwarz, M, Zhou, Z, Friedman, K, Carles, S, Claustres, M, Bozon, D, Verlingue, C, Ferec, C, Tzetis, M, Kanavakis, E, Cuppens, H, Bombieri, C, Pignatti, P, Sangiuolo, Fc, Jordanova, A, Kusic, J, Radojkovic, D, Sertic, J, Richter, D, Rukavina, A, Bjorck, E, Strandvik, B, Cardoso, H, Montgomery, M, Nakielna, B, Hughes, D, Estivill, X, Aznarez, I, Tullis, E, Tsui, L, Zielenski, J

مصطلحات موضوعية: Allele, Child, Preschool, Cystic Fibrosi, Cystic Fibrosis Transmembrane Conductance Regulator, DNA Mutational Analysi, Europe, Female, Gene Frequency, Human, Infant, Newborn, Male, Phenotype, Reverse Transcriptase Polymerase Chain Reaction, Sequence Deletion, Settore MED/03 - GENETICA MEDICA

Relation: info:eu-repo/semantics/altIdentifier/pmid/10798353; info:eu-repo/semantics/altIdentifier/wos/WOS:000086661100001; volume:106; issue:3; firstpage:259; lastpage:268; numberofpages:10; journal:HUMAN GENETICS; http://hdl.handle.net/2108/166508

الاتاحة: http://hdl.handle.net/2108/166508

المؤلفون: Dork, T, Macek, M, Mekus, F, Tummler, B, Tzountzouris, J, Casals, T, Krebsova, A, Koudova, M, Sakmaryova, I, Vavrova, V, Zemkova, D, Ginter, E, Petrova, NV, Ivaschenko, T, Baranov, V, Witt, M, Pogorzelski, A, Bal, J, Zekanowsky, C, Wagner, K, Stuhrmann, M, Bauer, I, Seydewitz, HH, Neumann, T, Jakubiczka, S, Kraus, C, Thamm, B, Nechiporenko, M, Livshits, L, Mosse, N, Tsukerman, G, Kadasi, L, Ravnik-Glavac, M, Glavac, D, Komel, R, Vouk, K, Kucinskas, V, Krumina, A, Teder, M, Kocheva, S, Efremov, GD, Onay, T, Kirdar, B, Malone, G, Schwarz, M, Zhou, ZQ, Friedman, KJ, Carles, S, Claustres, M, Bozon, D, Verlingue, C, Ferec, C, Tzetis, M, Kanavakis, E, Cuppens, Harry, Bombieri, C, Pignatti, PF, Sangiuolo, F, Jordanova, A, Kusic, J, Radojkovic, D, Sertic, J, Richter, D, Rukavina, AS, Bjorck, E, Strandvik, B, Cardoso, H, Montgomery, M, Nakielna, B, Hughes, D, Estivill, X, Aznarez, I, Tullis, E, Tsui, LC, Zielenski, J

مصطلحات موضوعية: transmembrane conductance regulator, identification, alleles, dna, recombination, heterogeneity, population, 90-percent, sequence, absence

Relation: Human Genetics vol:106 issue:3 pages:259-268; https://lirias.kuleuven.be/handle/123456789/159685

الاتاحة: https://lirias.kuleuven.be/handle/123456789/159685

المؤلفون: Dork, T Macek, M Mekus, F Tummler, B Tzountzouris, J and Casals, T Krebsova, A Koudova, M Sakmaryova, I Macek, M and Vavrova, V Zemkova, D Ginter, E Petrova, NV and Ivaschenko, T Baranov, V Witt, M Pogorzelski, A Bal, J and Zekanowsky, C Wagner, K Stuhrmann, M Bauer, I and Seydewitz, HH Neumann, T Jakubiczka, S Kraus, C Thamm, B and Nechiporenko, M Livshits, L Mosse, N Tsukerman, G and Kadasi, L Ravnik-Glavac, M Glavac, D Komel, R Vouk, K and Kucinskas, V Krumina, A Teder, M Kocheva, S Efremov, GD Onay, T Kirdar, B Malone, G Schwarz, M Zhou, ZQ and Friedman, KJ Carles, S Claustres, M Bozon, D and Verlingue, C Ferec, C Tzetis, M Kanavakis, E Cuppens, H and Bombieri, C Pignatti, PF Sangiuolo, F Jordanova, A and Kusic, J Radojkovic, D Sertic, J Richter, D Rukavina, AS and Bjorck, E Strandvik, B Cardoso, H Montgomery, M and Nakielna, B Hughes, D Estivill, X Aznarez, I Tullis, E and Tsui, LC Zielenski, J

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2127::a2eb34931b3ef03e41c7d846c93df28b
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3053081

المؤلفون: Kocheva, S. A.¹ svetlana.kocheva@t.mk, Martinova, K.¹, Antevska-Trajkova, Z.¹, Coneska-Jovanova, B.¹, Eftimov, A.², Dimovski, A. J.²

المصدر: Balkan Journal of Medical Genetics. Aug2016, Vol. 19 Issue 1, p91-94. 4p.

مصطلحات موضوعية: *LYMPHOBLASTIC leukemia treatment, *NIJMEGEN breakage syndrome, *MACEDONIANS, *MICROCEPHALY, *IMMUNODEFICIENCY, *DISEASE susceptibility