يعرض 1 - 20 نتائج من 42 نتيجة بحث عن '"Kluckow, E"', وقت الاستعلام: 0.79s تنقيح النتائج
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    Academic Journal

    مصطلحات موضوعية: Paediatrics

    Relation: Obstetrical and Gynecological Survey; Lindquist, A; Hui, L; Poulton, A; Kluckow, E; Hutchinson, B; Pertile, MD; Bonacquisto, L; Gugasyan, L; Kulkarni, A; Harraway, J; Howden, A; McCoy, R; Da Silva Costa, F; Menezes, M; et al., State-Wide Utilization and Performance of Traditional and Cell-Free DNA-Based Prenatal Testing Pathways: The Victorian Perinatal Record Linkage (PeRL) Study, Obstetrical and Gynecological Survey, 2021, 76 (1), pp. 3-5; http://hdl.handle.net/10072/408987

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    Conference

    مصطلحات موضوعية: Reproductive medicine

    جغرافية الموضوع: Berlin, Germany

    Time: 2019-10-12 to 2019-10-16

    Relation: Ultrasound in Obstetrics & Gynecology; 29th World Congress on Ultrasound in Obstetrics and Gynecology; Hui, L; Lindquist, A; Poulton, A; Kluckow, E; Hutchinson, B; Bonacquisto, L; Pertile, MD; Gugasyan, L; Kulkarni, A; Harraway, J; Howden, A; McCoy, R; da Silva Costa, F; Palma-Dias, R; Nisbet, D; et al., State-wide performance of traditional and cell-free DNA-based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study, Ultrasound in Obstetrics & Gynecology, 2019, 54 (S1), pp. 1-2; http://hdl.handle.net/10072/413894

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    Academic Journal

    Relation: Human Reproduction; Hui, L; Poulton, A; Kluckow, E; Lindquist, A; Hutchinson, B; Pertile, MD; Bonacquisto, L; Gugasyan, L; Kulkarni, A; Harraway, J; Howden, A; McCoy, R; Costa, FDS; Menezes, M; Palma-Dias, R; Nisbet, D; Martin, N; Bethune, M; Poulakis, Z; Halliday, J, A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort, Human Reproduction, 2020, 35 (3), pp. 694-704; http://hdl.handle.net/10072/410041

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    Academic Journal

    Relation: Ultrasound in Obstetrics and Gynecology; Lindquist, A; Hui, L; Poulton, A; Kluckow, E; Hutchinson, B; Pertile, MD; Bonacquisto, L; Gugasyan, L; Kulkarni, A; Harraway, J; Howden, A; McCoy, R; Da Silva Costa, F; Menezes, M; Palma-Dias, R; Nisbet, D; Martin, N; Bethune, M; Poulakis, Z; Halliday, J, State-wide utilization and performance of traditional and cell-free DNA-based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study, Ultrasound in Obstetrics and Gynecology, 2020, 56 (2), pp. 215-224; http://hdl.handle.net/10072/410057

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    Electronic Resource
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    Academic Journal

    المؤلفون: Kluckow, E, Krieser, DMZ, Slaa, M

    Relation: Kluckow, E., Krieser, D. M. Z. & Slaa, M. (2020). COVIDtoes in stay-at-home adolescents: An epiphenomenon?. EMERGENCY MEDICINE AUSTRALASIA, 32 (6), pp.1088-1090. https://doi.org/10.1111/1742-6723.13630.; http://hdl.handle.net/11343/276300

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    Electronic Resource

    مصطلحات الفهرس: monosomy X/di [Diagnosis], perinatal period, polyploidy, population research, prenatal diagnosis, prenatal period, prevalence, sex chromosome aberration/cn [Congenital Disorder], sex chromosome aberration/di [Diagnosis], spontaneous abortion, stillbirth, trisomy/cn [Congenital Disorder], trisomy/di [Diagnosis], trisomy 13/cn [Congenital Disorder], trisomy 13/di [Diagnosis], trisomy 16/cn [Congenital Disorder], trisomy 16/di [Diagnosis], trisomy 18/cn [Congenital Disorder], trisomy 18/di [Diagnosis], trisomy 21/cn [Congenital Disorder], trisomy 21/di [Diagnosis], DNA/ec [Endogenous Compound], trisomy 15/cn [Congenital Disorder], trisomy 15/di [Diagnosis], trisomy 22/cn [Congenital Disorder], trisomy 22/di [Diagnosis], article, 47,XXY syndrome/cn [Congenital Disorder], 47,XXY syndrome/di [Diagnosis], adult, amniocentesis, chorion villus sampling, chromosome aberration/cn [Congenital Disorder], chromosome aberration/di [Diagnosis], chromosome analysis, chromosome deletion 22q11/cn [Congenital Disorder], chromosome deletion 22q11/di [Diagnosis], cohort analysis, congenital malformation/cn [Congenital Disorder], controlled study, copy number variation, developmental stage, diagnostic value, female, fetus disease/cn [Congenital Disorder], fetus disease/di [Diagnosis], fetus echography, first trimester pregnancy, gene frequency, genetic screening, gestational age, heart disease/cn [Congenital Disorder], heart disease/di [Diagnosis], human, infant, live birth, major clinical study, maternal age, monosomy X/cn [Congenital Disorder], Article

    URL: https://repository.monashhealth.org/monashhealthjspui/handle/1/29241
    Human Reproduction
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    Electronic Resource
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    Academic Journal

    Relation: NHMRC/1105603; Kluckow, E., Halliday, J., Poulton, A., Lindquist, A., Hutchinson, B., Bethune, M., Bonacquisto, L., Da Silva Costa, F., Gugasyan, L., Harraway, J., Howden, A., Kulkarni, A., Martin, N., McCoy, R., Menezes, M., Nisbet, D., Palma-Dias, R., Pertile, M. D., Poulakis, Z. & Hui, L. (2019). 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. PRENATAL DIAGNOSIS, 39 (13), pp.1254-1261. https://doi.org/10.1002/pd.5577.; http://hdl.handle.net/11343/286583

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    Electronic Resource
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    Academic Journal
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    Electronic Resource
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    Electronic Resource