General practice experience of patient recall.
BMJPublished 12 January 1991Open access
Patricia R. McCartney, G.M. Cochrane
Citations10
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MedicineHealth Professions
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This microextraction procedure will allow immediate application of molecular genetic technology to direct newborn screening follow-up of disorders amenable to DNA diagnosis, such as sickle cell anemia, and may eventually permit primary DNA screening for specific mutations.
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Molecular confirmation of genotype from the original blotter would reduce the personnel costs associated with obtaining follow-up liquid blood specimens and would provide information to the family in a more timely and less equivocal manner.
