View in EDS HTML Full Text PDF Full Text

Implementation of a national rapid prenatal exome sequencing service in England: evaluation of service outcomes and factors associated with regional variation.

Saved in:
Bibliographic Details
Title: Implementation of a national rapid prenatal exome sequencing service in England: evaluation of service outcomes and factors associated with regional variation.
Authors: Ramakrishnan R; National Perinatal Epidemiology Unit, University of Oxford, Oxford, United Kingdom., Mallinson C; National Disease Registration Service, National Health Service England, London, United Kingdom., Hardy S; National Disease Registration Service, National Health Service England, London, United Kingdom., Broughan J; National Disease Registration Service, National Health Service England, London, United Kingdom., Blyth M; National Disease Registration Service, National Health Service England, London, United Kingdom., Melis G; National Disease Registration Service, National Health Service England, London, United Kingdom., Franklin C; National Disease Registration Service, National Health Service England, London, United Kingdom., Hill M; NHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, United Kingdom., Mellis R; NHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, United Kingdom., Wu WH; NHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, United Kingdom., Allen S; West Midlands Regional Genetics Service, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, United Kingdom., Chitty LS; NHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, United Kingdom., Knight M; National Perinatal Epidemiology Unit, University of Oxford, Oxford, United Kingdom.
Corporate Authors: EXPRESS Clinical Outcomes Group
Source: Frontiers in genetics [Front Genet] 2024 Nov 06; Vol. 15, pp. 1485306. Date of Electronic Publication: 2024 Nov 06 (Print Publication: 2024).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 39568676
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Implementation of a national rapid prenatal exome sequencing service in England: evaluation of service outcomes and factors associated with regional variation.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Ramakrishnan+R%22">Ramakrishnan R</searchLink>; National Perinatal Epidemiology Unit, University of Oxford, Oxford, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Mallinson+C%22">Mallinson C</searchLink>; National Disease Registration Service, National Health Service England, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Hardy+S%22">Hardy S</searchLink>; National Disease Registration Service, National Health Service England, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Broughan+J%22">Broughan J</searchLink>; National Disease Registration Service, National Health Service England, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Blyth+M%22">Blyth M</searchLink>; National Disease Registration Service, National Health Service England, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Melis+G%22">Melis G</searchLink>; National Disease Registration Service, National Health Service England, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Franklin+C%22">Franklin C</searchLink>; National Disease Registration Service, National Health Service England, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Hill+M%22">Hill M</searchLink>; NHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Mellis+R%22">Mellis R</searchLink>; NHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Wu+WH%22">Wu WH</searchLink>; NHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Allen+S%22">Allen S</searchLink>; West Midlands Regional Genetics Service, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Chitty+LS%22">Chitty LS</searchLink>; NHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Knight+M%22">Knight M</searchLink>; National Perinatal Epidemiology Unit, University of Oxford, Oxford, United Kingdom.
– Name: AuthorCorporate
  Label: Corporate Authors
  Group: Au
  Data: <searchLink fieldCode="CA" term="%22EXPRESS+Clinical+Outcomes+Group%22">EXPRESS Clinical Outcomes Group</searchLink>
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22101560621%22">Frontiers in genetics</searchLink> [Front Genet] 2024 Nov 06; Vol. 15, pp. 1485306. <i>Date of Electronic Publication: </i>2024 Nov 06 (<i>Print Publication: </i>2024).
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Research+Foundation%22">Frontiers Research Foundation </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101560621 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>1664-8021 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216648021%22">16648021 </searchLink><i>NLM ISO Abbreviation: </i>Front Genet <i>Subsets: </i>PubMed not MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=39568676
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.3389/fgene.2024.1485306
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 1485306
    Titles:
      – TitleFull: Implementation of a national rapid prenatal exome sequencing service in England: evaluation of service outcomes and factors associated with regional variation.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Ramakrishnan R
      – PersonEntity:
          Name:
            NameFull: Mallinson C
      – PersonEntity:
          Name:
            NameFull: Hardy S
      – PersonEntity:
          Name:
            NameFull: Broughan J
      – PersonEntity:
          Name:
            NameFull: Blyth M
      – PersonEntity:
          Name:
            NameFull: Melis G
      – PersonEntity:
          Name:
            NameFull: Franklin C
      – PersonEntity:
          Name:
            NameFull: Hill M
      – PersonEntity:
          Name:
            NameFull: Mellis R
      – PersonEntity:
          Name:
            NameFull: Wu WH
      – PersonEntity:
          Name:
            NameFull: Allen S
      – PersonEntity:
          Name:
            NameFull: Chitty LS
      – PersonEntity:
          Name:
            NameFull: Knight M
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 06
              M: 11
              Text: 2024 Nov 06
              Type: published
              Y: 2024
          Identifiers:
            – Type: issn-print
              Value: 1664-8021
          Numbering:
            – Type: volume
              Value: 15
          Titles:
            – TitleFull: Frontiers in genetics
              Type: main
ResultId 1