Search Results - Stomornjak-Vukadin, Meliha

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  1. 1
    Turner Syndrome: A Unique Mosaic Case with 45,X/47,XX,+21/46,XX Cell Lines

    Turner Syndrome: A Unique Mosaic Case with 45,X/47,XX,+21/46,XX Cell Lines by Mačkić-Đurović, PhD, Mirela, Stomornjak-Vukadin, MD, Meliha, Ibrulj, PhD, Slavka

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  2. 2
    Ten-year trends in prevalence of Down syndrome in a developing country: impact of the maternal age and prenatal screening

    Ten-year trends in prevalence of Down syndrome in a developing country: impact of the maternal age and prenatal screening by Kurtovic-Kozaric, Amina, Mehinovic, Lejla, Malesevic, Radmila, Mesanovic, Semir, Jaros, Tijana, Stomornjak-Vukadin, Meliha, Mackic-Djurovic, Mirela, Ibrulj, Slavica, Kurtovic-Basic, Ilvana, Kozaric, Mirza

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  3. 3
    Combined use of cytogenetic and molecular methods in prenatal diagnostics of chromosomal abnormalities

    Combined use of cytogenetic and molecular methods in prenatal diagnostics of chromosomal abnormalities by Stomornjak-Vukadin, Meliha, Kurtovic-Basic, Ilvana, Mehinovic, Lejla, Konjhodzic, Rijad

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  4. 4
    Use of Quantitative Fluorescent Polymerase Chain Reaction (QF PCR) in Prenatal Diagnostic of Fetal Aneuploidies in a 17 Month Period in Parallel with Karyotyping

    Use of Quantitative Fluorescent Polymerase Chain Reaction (QF PCR) in Prenatal Diagnostic of Fetal Aneuploidies in a 17 Month Period in Parallel with Karyotyping by Konjhodzic, Rijad, Dervovic, Edina, Kurtovic-Basic, Ilvana, Stomornjak-Vukadin, Meliha, Muhic, Adis, Baljevic, Sumeja, Pirnat-Gegic, Aida, Basic, Ejub, Bilalovic, Nurija

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  5. 5
    Diagnostics of common microdeletion syndromes using fluorescence in situ hybridization: single center experience in a developing country

    Diagnostics of common microdeletion syndromes using fluorescence in situ hybridization: single center experience in a developing country by Kurtovic-Kozaric, Amina, Mehinovic, Lejla, Stomornjak-Vukadin, Meliha, Kurtovic-Basic, Ilvana, Catibusic, Feriha, Kozaric, Mirza, Mesihovic-Dinarevic, Senka, Hasanhodzic, Mensuda, Glamuzina, Darinka

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  6. 6
    Turner Syndrome: A Unique Mosaic Case with 45,X/47,XX,+21/46,XX Cell Lines

    Turner Syndrome: A Unique Mosaic Case with 45,X/47,XX,+21/46,XX Cell Lines by Mačkić-Đurović, Mirela, Stomornjak-Vukadin, Meliha, Ibrulj, Slavka

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