Hasil Pencarian - Lyn S Chitty

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  1. 1
    Women's Experiences and Preferences for Service Delivery of Non-Invasive Prenatal Testing for Aneuploidy in a Public Health Setting: A Mixed Methods Study.

    Women's Experiences and Preferences for Service Delivery of Non-Invasive Prenatal Testing for Aneuploidy in a Public Health Setting: A Mixed Methods Study. oleh Celine Lewis, Melissa Hill, Lyn S Chitty

    Diterbitkan 2016-01-01
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  2. 2
    Clinical, social and ethical issues associated with non-invasive prenatal testing for aneuploidy

    Clinical, social and ethical issues associated with non-invasive prenatal testing for aneuploidy oleh Blanche Griffin, Samantha Edwards, Lyn S. Chitty, Celine Lewis

    Diterbitkan 2018-01-01
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  3. 3
    Development and evaluation of training resources to prepare health professionals for counselling pregnant women about non-invasive prenatal testing for Down syndrome: a mixed methods study

    Development and evaluation of training resources to prepare health professionals for counselling pregnant women about non-invasive prenatal testing for Down syndrome: a mixed metho... oleh Kerry Oxenford, Rebecca Daley, Celine Lewis, Melissa Hill, Lyn S. Chitty

    Diterbitkan 2017-04-01
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  4. 4
    Model-based analysis of costs and outcomes of non-invasive prenatal testing for Down's syndrome using cell free fetal DNA in the UK National Health Service.

    Model-based analysis of costs and outcomes of non-invasive prenatal testing for Down's syndrome using cell free fetal DNA in the UK National Health Service. oleh Stephen Morris, Saffron Karlsen, Nancy Chung, Melissa Hill, Lyn S Chitty

    Diterbitkan 2014-01-01
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  5. 5
    Implementing prenatal diagnosis based on cell-free fetal DNA: accurate identification of factors affecting fetal DNA yield.

    Implementing prenatal diagnosis based on cell-free fetal DNA: accurate identification of factors affecting fetal DNA yield. oleh Angela N Barrett, Bernhard G Zimmermann, Darrell Wang, Andrew Holloway, Lyn S Chitty

    Diterbitkan 2011-01-01
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  6. 6
    Evaluation of a novel assay for detection of the fetal marker RASSF1A: facilitating improved diagnostic reliability of noninvasive prenatal diagnosis.

    Evaluation of a novel assay for detection of the fetal marker RASSF1A: facilitating improved diagnostic reliability of noninvasive prenatal diagnosis. oleh Helen E White, Carolyn L Dent, Victoria J Hall, John A Crolla, Lyn S Chitty

    Diterbitkan 2012-01-01
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  7. 7
    Evaluation of allelic expression of imprinted genes in adult human blood.

    Evaluation of allelic expression of imprinted genes in adult human blood. oleh Jennifer M Frost, Dave Monk, Taita Stojilkovic-Mikic, Kathryn Woodfine, Lyn S Chitty, Adele Murrell, Philip Stanier, Gudrun E Moore

    Diterbitkan 2010-10-01
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  8. 8
    "We might get a lot more families who will agree": Muslim and Jewish perspectives on less invasive perinatal and paediatric autopsy.

    "We might get a lot more families who will agree": Muslim and Jewish perspectives on less invasive perinatal and paediatric autopsy. oleh Celine Lewis, Zahira Latif, Melissa Hill, Megan Riddington, Monica Lakhanpaul, Owen J Arthurs, John C Hutchinson, Lyn S Chitty, Neil J Sebire

    Diterbitkan 2018-01-01
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  9. 9
    A case-control study of maternal periconceptual and pregnancy recreational drug use and fetal malformation using hair analysis.

    A case-control study of maternal periconceptual and pregnancy recreational drug use and fetal malformation using hair analysis. oleh Anna L David, Andrew Holloway, Louise Thomasson, Argyro Syngelaki, Kypros Nicolaides, Roshni R Patel, Brian Sommerlad, Amie Wilson, William Martin, Lyn S Chitty

    Diterbitkan 2014-01-01
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  10. 10
    Evaluation of Array Comparative genomic Hybridisation in prenatal diagnosis of fetal anomalies: a multicentre cohort study with cost analysis and assessment of patient, health professional and commissioner preferences for array comparative genomic hybridisation

    Evaluation of Array Comparative genomic Hybridisation in prenatal diagnosis of fetal anomalies: a multicentre cohort study with cost analysis and assessment of patient, health prof... oleh Stephen C Robson, Lyn S Chitty, Stephen Morris, Talitha Verhoef, Gareth Ambler, Diana G Wellesley, Ruth Graham, Claire Leader, Jane Fisher, John A Crolla

    Diterbitkan 2017-02-01
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  11. 11
    Minimally invasive autopsy for fetuses and children based on a combination of post-mortem MRI and endoscopic examination: a feasibility study

    Minimally invasive autopsy for fetuses and children based on a combination of post-mortem MRI and endoscopic examination: a feasibility study oleh Celine Lewis, John C Hutchinson, Megan Riddington, Melissa Hill, Owen J Arthurs, Jane Fisher, Angie Wade, Caroline J Doré, Lyn S Chitty, Neil J Sebire

    Diterbitkan 2019-08-01
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  12. 12
    Preferences for coordinated care for rare diseases: discrete choice experiment

    Preferences for coordinated care for rare diseases: discrete choice experiment oleh Stephen Morris, Holly Walton, Amy Simpson, Kerry Leeson-Beevers, Lara Bloom, Amy Hunter, Angus I. G. Ramsay, Naomi J. Fulop, Lyn S. Chitty, Joe Kai, Alastair G. Sutcliffe, Maria Kokocinska, Larissa Kerecuk, Christine A. Taylor, Pei Li Ng

    Diterbitkan 2024-09-01
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  13. 13
    Experiences of coordinated care for people in the UK affected by rare diseases: cross-sectional survey of patients, carers, and healthcare professionals

    Experiences of coordinated care for people in the UK affected by rare diseases: cross-sectional survey of patients, carers, and healthcare professionals oleh Holly Walton, Pei Li Ng, Amy Simpson, Lara Bloom, Lyn S. Chitty, Naomi J. Fulop, Amy Hunter, Jennifer Jones, Joe Kai, Larissa Kerecuk, Maria Kokocinska, Kerry Leeson-Beevers, Sharon Parkes, Angus I. G. Ramsay, Alastair Sutcliffe, Christine Taylor, Stephen Morris

    Diterbitkan 2023-11-01
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  14. 14
    Co-ordinated care for people affected by rare diseases: the CONCORD mixed-methods study

    Co-ordinated care for people affected by rare diseases: the CONCORD mixed-methods study oleh Stephen Morris, Emma Hudson, Lara Bloom, Lyn S Chitty, Naomi J Fulop, Amy Hunter, Jennifer Jones, Joe Kai, Larissa Kerecuk, Maria Kokocinska, Kerry Leeson-Beevers, Pei Li Ng, Sharon Parkes, Angus IG Ramsay, Amy Simpson, Alastair Sutcliffe, Christine Taylor, Holly Walton

    Diterbitkan 2022-03-01
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  15. 15
    Delivery of a national prenatal exome sequencing service in England: a mixed methods study exploring healthcare professionals’ views and experiences

    Delivery of a national prenatal exome sequencing service in England: a mixed methods study exploring healthcare professionals’ views and experiences oleh Michelle Peter, Michelle Peter, Rhiannon Mellis, Rhiannon Mellis, Hannah McInnes-Dean, Morgan Daniel, Morgan Daniel, Holly Walton, Jane Fisher, Kerry Leeson-Beevers, Stephanie Allen, Emma L. Baple, Emma L. Baple, Ana Beleza-Meireles, Marta Bertoli, Jennifer Campbell, Natalie Canham, Deirdre Cilliers, Jan Cobben, Jacqueline Eason, Victoria Harrison, Muriel Holder-Espinasse, Alison Male, Sahar Mansour, Alec McEwan, Soo-Mi Park, Audrey Smith, Alison Stewart, Dagmar Tapon, Pradeep Vasudevan, Denise Williams, Wing Han Wu, Wing Han Wu, Lyn S. Chitty, Lyn S. Chitty, Melissa Hill, Melissa Hill

    Diterbitkan 2024-06-01
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  16. 16
    An exploratory open-label multicentre phase I/II trial evaluating the safety and efficacy of postnatal or prenatal and postnatal administration of allogeneic expanded fetal mesenchymal stem cells for the treatment of severe osteogenesis imperfecta in infants and fetuses: the BOOSTB4 trial protocol

    An exploratory open-label multicentre phase I/II trial evaluating the safety and efficacy of postnatal or prenatal and postnatal administration of allogeneic expanded fetal mesench... oleh Anna L David, Mats Johansson, Magnus Westgren, Belinda Crowe, Dick Oepkes, Melissa Hill, Lyn S Chitty, Catherine DeVile, Peter Lindgren, Eva Åström, Cecilia Götherström, Nils-Eric Sahlin, Rachel L Sagar, Annabelle Forsmark, Vera Franzen, Göran Hermeren, Caroline Lindemans, Wouter Nijhuis, Mirko Rehberg, Ralph Sakkers, O Semler, Mikael Sundin, Lilian Walther-Jallow, E J T Joanne Verweij

    Diterbitkan 2024-06-01
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  17. 17
    Optimising Exome Prenatal Sequencing Services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS Genomic Medicine Service [version 2; peer review: 2 approved]

    Optimising Exome Prenatal Sequencing Services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS Genomic Medicine Service [version 2; peer review: 2... oleh Melissa Hill, Sian Ellard, Naomi Fulop, Jane Fisher, Mark Kroese, Marian Knight, Kerry Leeson-Beevers, Jean Ledger, Dominic McMullan, Alec McEwan, Stephen Morris, Rhiannon Mellis, Dagmar Tapon, Michael Parker, Laura Blackburn, Holly Walton, Emma Baple, Caroline Lafarge, Asya Choudry, Emma Smith, Michelle Peter, Hannah McInnes-Dean, Lauren Roberts, Rema Ramakrishnan, Sarah L. Wynn, Beverly Searle, Lyn S. Chitty, Wing Han Wu

    Diterbitkan 2022-07-01
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