Search Results - TARDY, Erika P

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  1. 1
    A rapid technique for detecting chromosomal aneuploidy in early childhood by fluorescence in situ hybridisation

    A rapid technique for detecting chromosomal aneuploidy in early childhood by fluorescence in situ hybridisation by Tardy, E P, Tóth, A

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  2. 2
    AZFc deletion detected in a newborn with prenatally diagnosed Yq deletion

    AZFc deletion detected in a newborn with prenatally diagnosed Yq deletion by Tóth, András, Tardy, Erika P., Gombos, Sándor, Hajdu, Krisztina, Bátorfi, József, Krausz, Csilla

    Published in Prenatal diagnosis
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  3. 3
    Fluorescence in situ hybridization of chorionic interphase cells for prenatal screening of Down syndrome

    Fluorescence in situ hybridization of chorionic interphase cells for prenatal screening of Down syndrome by TOTH, Andras, TARDY, Erika P, HAJDU, Krisztina, BATORFI, Jozsef, DOSZPOD, Jozsef, EGYED, Jeno, GATI, Istvan

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    Prenatal Exclusion of Segmental Trisomy in Familial Chromosome 21 Pericentric Inversion by Fluorescencein situ Hybridization

    Prenatal Exclusion of Segmental Trisomy in Familial Chromosome 21 Pericentric Inversion by Fluorescencein situ Hybridization by Tardy, Erika P., Tóth, András, Kosztolányi, György

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  5. 5
    Prenatal Exclusion of Segmental Trisomy in Familial Chromosome 21 Pericentric Inversion by Fluorescence in situ Hybridization

    Prenatal Exclusion of Segmental Trisomy in Familial Chromosome 21 Pericentric Inversion by Fluorescence in situ Hybridization by Tardy, Erika P., Tóth, András, Kosztolányi, György

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