Rezultati pretrage - Melody Menezes

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  1. 1
    Prenatal diagnosis following preimplantation genetic testing for monogenic conditions: a single centre record linkage study

    Prenatal diagnosis following preimplantation genetic testing for monogenic conditions: a single centre record linkage study od Alice Poulton, Melody Menezes, Tristan Hardy, Sarah J. Lewis, Lisa Hui

    Izdano 2025
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  2. 2
    Cell-free fetal DNA testing in singleton IVF conceptions

    Cell-free fetal DNA testing in singleton IVF conceptions od Timothy Lee, Daniel L. Rolnik, Melody Menezes, Andrew McLennan, Fabrício da Silva Costa

    Izdano 2018
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  3. 3
    OC11.02: The importance of ultrasound preceding non‐invasive prenatal testing for fetal chromosomal abnormalities

    OC11.02: The importance of ultrasound preceding non‐invasive prenatal testing for fetal chromosomal abnormalities od Imogen Brown, Shavi Fernando, Melody Menezes, Fabrício da Silva Costa, Jayshree Ramkrishna, S. Meagher, Daniel L. Rolnik

    Izdano 2020
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  4. 4
    The importance of ultrasound preceding cell‐free <scp>DNA</scp> screening for fetal chromosomal abnormalities

    The importance of ultrasound preceding cell‐free <scp>DNA</scp> screening for fetal chromosomal abnormalities od Imogen Brown, Shavi Fernando, Melody Menezes, Fabrício da Silva Costa, Jayshree Ramkrishna, Simon Meagher, Daniel L. Rolnik

    Izdano 2020
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  5. 5
    Outcomes following the detection of fetal edema in early pregnancy prior to non‐invasive prenatal testing

    Outcomes following the detection of fetal edema in early pregnancy prior to non‐invasive prenatal testing od Jayshree Ramkrishna, Melody Menezes, Kedar Humnabadkar, Cheryl Tse, Maria Maxfield, Fabrício da Silva Costa, Daniel L. Rolnik, Simon Meagher

    Izdano 2020
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  6. 6
    Experiences of prenatal diagnosis and decision‐making about termination of pregnancy: A qualitative study

    Experiences of prenatal diagnosis and decision‐making about termination of pregnancy: A qualitative study od Jan Hodgson, Penelope Pitt, Sylvia A. Metcalfe, Jane Halliday, Melody Menezes, Jane Fisher, Chriselle Hickerton, Kerry Petersen, Belinda McClaren

    Izdano 2016
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  7. 7
    The accuracy of cell‐free <scp>DNA</scp> screening for fetal segmental copy number variants: A systematic review and meta‐analysis

    The accuracy of cell‐free <scp>DNA</scp> screening for fetal segmental copy number variants: A systematic review and meta‐analysis od Yvette Raymond, Melissa L. Acreman, Sofia Bussolaro, Ben W. Mol, Shavi Fernando, Melody Menezes, Fabrício da Silva Costa, Ilaria Fantasia, Daniel L. Rolnik

    Izdano 2023
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  8. 8
    State‐wide utilization and performance of traditional and cell‐free DNA‐based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study

    State‐wide utilization and performance of traditional and cell‐free DNA‐based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study od Anthea Lindquist, Lisa Hui, Alice Poulton, Eliza Kluckow, B. Hutchinson, Mark D. Pertile, L Bonacquisto, Lucy Gugasyan, Abhijit Kulkarni, James Harraway, A. Howden, R. McCoy, Fabrício da Silva Costa, Melody Menezes, Ricardo Palma‐Dias, Debbie Nisbet, Nicholas G. Martin, M. Bethune, Zeffie Poulakis, Jane Halliday

    Izdano 2019
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  9. 9
    Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio‐economic status in Victoria, Australia: A population‐based cohort study from 2015 to 2016

    Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio‐economic status in Victoria, Australia: A population‐based cohort study from 2015 to 2016 od Eliza Kluckow, Jane Halliday, Alice Poulton, Anthea Lindquist, B. Hutchinson, Michael Bethune, L Bonacquisto, Fabrício da Silva Costa, Lucy Gugasyan, James Harraway, A. Howden, Abhijit Kulkarni, Nicole J. Martin, Richard McCoy, Melody Menezes, Debbie Nisbet, Ricardo Palma‐Dias, Mark D. Pertile, Zeffie Poulakis, Lisa Hui

    Izdano 2019
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  10. 10
    A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort

    A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort od Lisa Hui, Alice Poulton, Eliza Kluckow, Anthea Lindquist, B. Hutchinson, Mark D. Pertile, L Bonacquisto, Lucy Gugasyan, Abhijit Kulkarni, James Harraway, A. Howden, Richard McCoy, Fabrício da Silva Costa, Melody Menezes, Ricardo Palma‐Dias, Debbie Nisbet, Nicole J. Martin, Michael Bethune, Zeffie Poulakis, Jane Halliday

    Izdano 2020
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  11. 11
    State-Wide Utilization and Performance of Traditional and Cell-Free DNA-Based Prenatal Testing Pathways: The Victorian Perinatal Record Linkage (PeRL) Study

    State-Wide Utilization and Performance of Traditional and Cell-Free DNA-Based Prenatal Testing Pathways: The Victorian Perinatal Record Linkage (PeRL) Study od Anthea Lindquist, Lisa Hui, Alice Poulton, Eliza Kluckow, B. Hutchinson, Mark D. Pertile, L Bonacquisto, Lucy Gugasyan, Abhijit Kulkarni, James Harraway, A. Howden, R. McCoy, Fabrício da Silva Costa, Melody Menezes, Ricardo Palma‐Dias, Debbie Nisbet, Nicholas G. Martin, M. Bethune, Zeffie Poulakis, Jane Halliday

    Izdano 2021
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  12. 12
    DNA Evidence in Property Crimes: An Analysis of More than 4200 Samples Processed by the Brazilian Federal PoliceForensic Genetics Laboratory

    DNA Evidence in Property Crimes: An Analysis of More than 4200 Samples Processed by the Brazilian Federal PoliceForensic Genetics Laboratory od Gustavo Chemale, C. B. V. Carvalho, Jeferson Loureiro Badaraco, Ana Paula Vieira de Castro, S. M. Aguiar, Ronaldo Carneiro da Silva, L. H. Fassio, Bruno Rodrigues Trindade, Clarice Medeiros, Renata Silva Paiva, Aline Costa Minervino, Jorge Marcelo de Freitas, Kátia Michelin, H. B. Lima, Guilherme Silveira Jacques, Melody Menezes, Renato Teodoro Ferreira de Paranaíba

    Izdano 2016
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