Search Results - Sukarova-Angelovska, E

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  1. 1
    Duplication of chromosome 16p13.11-p12.3 with different expressions in the same family

    Duplication of chromosome 16p13.11-p12.3 with different expressions in the same family by Pop-Jordanova, N, Zorcec, T, Sukarova-Angelovska, E

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  2. 2
    THE INCIDENCE AND TYPE OF CHROMOSOMAL TRANSLOCATIONS FROM PRENATAL DIAGNOSIS OF 3800 PATIENTS IN THE REPUBLIC OF MACEDONIA

    THE INCIDENCE AND TYPE OF CHROMOSOMAL TRANSLOCATIONS FROM PRENATAL DIAGNOSIS OF 3800 PATIENTS IN THE REPUBLIC OF MACEDONIA by Vasilevska, M., Ivanovska, E., Kubelka Sabit, K., Sukarova-Angelovska, E., Dimeska, G.

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  3. 3
    Phenotypic Variations in Wolfhirschhorn Syndrome

    Phenotypic Variations in Wolfhirschhorn Syndrome by E, Sukarova-Angelovska, M, Kocova, V, Sabolich, S, Palcevska, N, Angelkova

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  4. 4
    Myopathic form of carnitine palmitoyltransferase II deficiency – Case report

    Myopathic form of carnitine palmitoyltransferase II deficiency – Case report by Angelkova, N, Sukarova-Angelovska, E, Kocova, M, Duma, F, Sabolic, V

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  5. 5
    The Many Faces of Oral-Facial-Digital Syndrome

    The Many Faces of Oral-Facial-Digital Syndrome by Sukarova-Angelovska, E, Angelkova, N, Palcevska-Kocevska, S, Kocova, M

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  6. 6
    Phenotypic variations in wolf-hirschhorn syndrome

    Phenotypic variations in wolf-hirschhorn syndrome by Sukarova-Angelovska, E, Kocova, M, Sabolich, V, Palcevska, S, Angelkova, N

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  7. 7
    HLA-DR-DQ haplotypes and type 1 diabetes in Macedonia

    HLA-DR-DQ haplotypes and type 1 diabetes in Macedonia by Ilonen, Jorma, Kocova, Mirjana, Lipponen, Kati, Sukarova-Angelovska, Elena, Jovanovska, Aleksandra, Knip, Mikael

    Published in Human immunology
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  8. 8
    P03.6 Myotonic myopathy-Swartz-Jampel Syndrome 1a-case report

    P03.6 Myotonic myopathy-Swartz-Jampel Syndrome 1a-case report by Angelkova, N., Angelovska, E. Sukarova, Demerdziev, M., Lekovska, O., Avramovska, V. Sabolic, Duma, F.

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  9. 9
    Missense variant contribution to USP9X-female syndrome

    Missense variant contribution to USP9X-female syndrome by Jolly, Lachlan A., Parnell, Euan, Gardner, Alison E., Corbett, Mark A., Pérez-Jurado, Luis A., Shaw, Marie, Lesca, Gaetan, Keegan, Catherine, Schneider, Michael C., Griffin, Emily, Maier, Felicitas, Kiss, Courtney, Guerin, Andrea, Crosby, Kathleen, Rosenbaum, Kenneth, Tanpaiboon, Pranoot, Whalen, Sandra, Keren, Boris, McCarrier, Julie, Basel, Donald, Sadedin, Simon, White, Susan M., Delatycki, Martin B., Kleefstra, Tjitske, Küry, Sébastien, Brusco, Alfredo, Sukarova-Angelovska, Elena, Trajkova, Slavica, Yoon, Sehoun, Wood, Stephen A., Piper, Michael, Penzes, Peter, Gecz, Jozef

    Published in Npj genomic medicine
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  10. 10
    Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions

    Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions by Ferraris, Alessandro, Bernardini, Laura, Sabolic Avramovska, Vesna, Zanni, Ginevra, Loddo, Sara, Sukarova-Angelovska, Elena, Parisi, Valentina, Capalbo, Anna, Tumini, Stefano, Travaglini, Lorena, Mancini, Francesca, Duma, Filip, Barresi, Sabina, Novelli, Antonio, Mercuri, Eugenio, Tarani, Luigi, Bertini, Enrico, Dallapiccola, Bruno, Valente, Enza Maria

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