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dc.contributor.authorBerghs, Mariaen
dc.contributor.authorAtkin, Karlen
dc.contributor.authorDyson, Simonen
dc.date.accessioned2015-02-09T14:23:09Z
dc.date.available2015-02-09T14:23:09Z
dc.date.issued2014
dc.identifier.citationBerghs, M., Atkin, K. and Dyson, S.M. (2014) Involving Fathers in Ante-Natal Screening for Sickle Cell Disorders: Improving Informed Decision-Making Research for Patient Benefit Report PB-PG-0610-22196. York: University of Yorken
dc.identifier.urihttp://hdl.handle.net/2086/10632
dc.description.abstractThere are many reasons why fathers find it difficult to be involved in ante-natal screening for sickle cell disorders. Some are the consequence of disadvantage and inequalities, others are associated with how services are organised. Men’s perceptions about the relevance of screening are equally important, along with their relationship with their partners and families. Examples of good practice also exist and we can learn from these. Our report includes findings and recommendations for policy and practice.en
dc.language.isoenen
dc.publisherUniversity of Yorken
dc.subjectsickle cellen
dc.subjectante-natal screeningen
dc.subjectfathersen
dc.subjectreproductive technologyen
dc.titleInvolving Fathers in Ante-Natal Screening for Sickle Cell Disorders: Improving Informed Decision-Makingen
dc.typeOtheren
dc.researchgroupUnit for the Social Study of Thalassaemia and Sickle Cellen
dc.peerreviewedNoen
dc.explorer.multimediaNoen
dc.funderNational Institute for Health Research, Research for Patient Benefiten
dc.projectidResearch for Patient Benefit PB-PG-0610-22196en
dc.researchinstituteInstitute for Allied Health Sciences Researchen
dc.researchinstituteInstitute of Health, Health Policy and Social Careen


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