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Pediatrics|December 26, 2012
Obtaining consent from both parents for pediatric research: what does "reasonably available" mean?Daniel K Nelson, Debra Skinner, Sonia Guarda, et al.Health Matrix (Cleveland, Ohio : 1991)|May 23, 2009
The blurred distinction between treatable and untreatable conditions in newborn screeningDonald B BaileyMental Retardation and Developmental Disabilities Research Reviews|March 3, 2004
Newborn screening for fragile X syndromeDonald B BaileyMolecular Diagnosis & Therapy|May 4, 2022
A Window of Opportunity for Newborn ScreeningDonald B BaileyIntellectual and Developmental Disabilities|July 6, 2010
Narrating disability, narrating religious practice: reconciliation and fragile X syndromeMarsha Michie, Debra SkinnerMedical Anthropology|October 19, 2007
Experiencing the genetic body: parents' encounters with pediatric clinical geneticsKelly Raspberry, Debra SkinnerSociology of Health & Illness|November 9, 2010
Enacting genetic responsibility: experiences of mothers who carry the fragile X geneKelly Raspberry, Debra SkinnerSocial Science & Medicine (1982)|February 22, 2011
Negotiating desires and options: how mothers who carry the fragile X gene experience reproductive decisionsKelly Amanda Raspberry, Debra SkinnerMental Retardation and Developmental Disabilities Research Reviews|November 6, 2007
Sociocultural studies of families of children with intellectual disabilitiesDebra Skinner, Thomas S WeisnerJournal of Genetic Counseling|October 22, 2008
How parents search, interpret, and evaluate genetic information obtained from the internetMyra I Roche, Debra SkinnerPageof 18