Prenatal Diagnosis, 0197-3851

Journal

1 - 10 out of 33Page size: 10

Publications

  1. 2020
  2. Accepted/In press

    Evolution of a prenatal genetic clinic – A ten-year cohort study

    Mark Kilby, 24 Jan 2020, (Accepted/In press) In : Prenatal Diagnosis.

    Research output: Contribution to journal › Article

  3. 2019
  4. Published

    Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases

    Hsu Chong, R. Katie Morris & Mark Kilby, Nov 2019, In : Prenatal Diagnosis. 39, 12, p. 1064-1069 6 p.

    Research output: Contribution to journal › Article

  5. Published

    MicroRNA changes in maternal serum from pregnancies complicated by twin-twin transfusion syndrome: a discovery study

    Andrew Beggs, R. Katie Morris & Mark Kilby, 16 Jul 2019, In : Prenatal Diagnosis. 39, 8, p. 616-634

    Research output: Contribution to journal › Article

  6. 2017
  7. Published

    Parental experiences of prenatal whole exome sequencing (WES) in cases of ultrasound diagnosed fetal structural anomaly

    Mark Kilby & Sheila Greenfield, 10 Nov 2017, In : Prenatal Diagnosis. 37, 12, p. 1225-1231 7 p.

    Research output: Contribution to journal › Article

  8. Published

    Association of maternal serum PAPP-A levels, nuchal translucency and crown–rump length in first trimester with adverse pregnancy outcomes: retrospective cohort study

    Mark Kilby & R. Katie Morris, Jul 2017, In : Prenatal Diagnosis. 37, 7, p. 705-711 7 p.

    Research output: Contribution to journal › Article

  9. 2016
  10. E-pub ahead of print

    Association of serum PAPP-A levels in first trimester with small-for-gestational-age and adverse pregnancy outcomes: systematic review and meta-analysis

    R. Katie Morris & Mark Kilby, 23 Dec 2016, In : Prenatal Diagnosis.

    Research output: Contribution to journal › Article

  11. E-pub ahead of print

    Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives

    Mark Kilby, Sheila Greenfield, 18 Sep 2016, In : Prenatal Diagnosis.

    Research output: Contribution to journal › Article

  12. 2015
  13. Published

    A review of pregnancies complicated by congenital sacrococcygeal teratoma in the West Midlands region over an 18-year period: population-based, cohort study

    Anthony Lander & Mark Kilby, Nov 2015, In : Prenatal Diagnosis. 35, 11, p. 1037-47 11 p.

    Research output: Contribution to journal › Article

  14. Published

    Fetal brain injury in survivors of twin pregnancies complicated by demise of one twin as assessed by in utero MR imaging

    Mark Kilby, Jun 2015, In : Prenatal Diagnosis. 35, 6, p. 583-91 9 p.

    Research output: Contribution to journal › Article

  15. 2014
  16. Published

    Chromosomal microarray analysis allows prenatal detection of low level mosaic autosomal aneuploidy

    Fiona Mackie, Mark Kilby, May 2014, In : Prenatal Diagnosis. 34, 5, p. 505-7 3 p.

    Research output: Contribution to journal › Article

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