Hasil Pencarian - Beata Nowakowska

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  1. 1
    The role of ultrasound and genetic counsel in prenatal diagnosis of split hand/foot malformation with long bone deficiency

    The role of ultrasound and genetic counsel in prenatal diagnosis of split hand/foot malformation with long bone deficiency oleh Anna Kucińska-Chahwan, Dominika Szczęśniak, Beata Nowakowska, Tomasz Roszkowski

    Diterbitkan 2019-07-01
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  2. 2
    The Presence of Mycotoxins in Human Amniotic Fluid

    The Presence of Mycotoxins in Human Amniotic Fluid oleh Karolina Gromadzka, Jakub Pankiewicz, Monika Beszterda, Magdalena Paczkowska, Beata Nowakowska, Rafał Kocyłowski

    Diterbitkan 2021-06-01
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  3. 3
    Multiple occurrence of psychomotor retardation and recurrent miscarriages in a family with a submicroscopic reciprocal translocation t(7;17)(p22;p13.2)

    Multiple occurrence of psychomotor retardation and recurrent miscarriages in a family with a submicroscopic reciprocal translocation t(7;17)(p22;p13.2) oleh Magdalena Pasińska, Ewelina Łazarczyk, Katarzyna Jułga, Magdalena Bartnik-Głaska, Beata Nowakowska, Olga Haus

    Diterbitkan 2018-08-01
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  4. 4
    Association between the Concentrations of Essential and Toxic Elements in Mid-Trimester Amniotic Fluid and Fetal Chromosomal Abnormalities in Pregnant Polish Women

    Association between the Concentrations of Essential and Toxic Elements in Mid-Trimester Amniotic Fluid and Fetal Chromosomal Abnormalities in Pregnant Polish Women oleh Joanna Suliburska, Jakub Pankiewicz, Adam Sajnóg, Magdalena Paczkowska, Beata Nowakowska, Ewa Bakinowska, Danuta Barałkiewicz, Rafał Kocyłowski

    Diterbitkan 2022-04-01
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  5. 5
    How does terminal 21q22 deletion really manifest? Delineation based on prenatal diagnosis and literature review

    How does terminal 21q22 deletion really manifest? Delineation based on prenatal diagnosis and literature review oleh Miroslaw Wielgos, Przemyslaw Kosinski, Piotr Jedrzejak, Małgorzata Krajewska-Walasek, Magdalena Bartnik-Glaska, Beata Nowakowska, Aleksandra Jezela-Stanek

    Diterbitkan 2021-11-01
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  6. 6
    P217: Abnormalities of TBX1 result in broad overlapping features of 22q11.2 deletion syndrome

    P217: Abnormalities of TBX1 result in broad overlapping features of 22q11.2 deletion syndrome oleh Donna McDonald-McGinn, Victoria Giunta, T. Blaine Crowley, Daniel McGinn, Lydia Rockart, Audrey Green, Beverly Emanuel, Rosemarie Smith, Ellen Moran, Maciej Geremek, Elaine Zackai, Beata Nowakowska

    Diterbitkan 2024-01-01
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