A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.
about
A qualitative exploration of mothers' and fathers' experiences of having a child with Klinefelter syndrome and the process of reaching this diagnosis.When the cystic fibrosis label does not fit: a modified uncertainty theoryNarrating disability, narrating religious practice: reconciliation and fragile X syndrome.What's at stake? Genetic information from the perspective of people with epilepsy and their family members.Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome.Variants of unknown significance on chromosomal microarray analysis: parental perspectives.Known unknowns: building an ethics of uncertainty into genomic medicine"What does it mean?": uncertainties in understanding results of chromosomal microarray testing.Policy considerations in designing a fragile X population screening program"Nothing is absolute in life": understanding uncertainty in the context of psychiatric genetic counseling from the perspective of those with serious mental illness.The role of hope in adaptation to uncertainty: the experience of caregivers of children with Down syndromeSupporting family adaptation to presymptomatic and "untreatable" conditions in an era of expanded newborn screeningUnderstanding the Psychosocial Effects of WES Test Results on Parents of Children with Rare Diseases.Patients-in-waiting: Living between sickness and health in the genomics era.Postnatal screening for Klinefelter syndrome: is there a rationale?"Set in Stone" or "Ray of Hope": Parents' Beliefs About Cause and Prognosis After Genomic Testing of Children Diagnosed with ASD.Families dealing with the uncertainty of genetic disorders: the case of Neurofibromatosis Type 1.Shifting uncertainties in the pre-diagnostic trajectory of early-onset dementia.Genetic counseling, activism and 'genotype-first' diagnosis of developmental disorders.Hyperdiagnostics: postcolonial utopics of race-based biomedicine.The Spillover of Genomic Testing Results in Families: Same Variant, Different Logics.Patient and family trajectories of mitochondrial disease: diversity, uncertainty and genetic risk.Investigating Uncertainty in Genetic Counseling Encounters: Managing Information About Genetic Cancer Risk.Spirituality, Illness Unpredictability, and Math Anxiety Effects on Negative Affect and Affect-Management Coping for Individuals Diagnosed with Alpha-1 Antitrypsin Deficiency.Gene worlds.Mothers' appreciation of chromosomal microarray analysis for autism spectrum disorder.Parents' Perspectives on Variants of Uncertain Significance from Chromosome Microarray Analysis."They Can't Find Anything Wrong with Him, Yet": Mothers' experiences of parenting an infant with a prenatally diagnosed copy number variant (CNV)."Possibly positive or certainly uncertain?": participants' responses to uncertain diagnostic results from exome sequencing.
P2860
Q30559709-41E25536-5793-453E-9C2A-762910136167Q33828144-3E0C8E56-D482-42E7-B981-F1DE5DC83EABQ35086435-DF62FABA-8A93-4D64-A723-1B9C37E48FBFQ35184580-F6554C6C-9F6F-43A5-BCA1-3012906E14DBQ35695460-42B3C29C-957A-4758-9C4E-9EF1EC0FDB39Q36054612-B5F424EA-B56E-47F0-A5E6-6F02D83E68BAQ36120680-A4DBC369-13E7-47E9-A40D-633916370DB1Q36241921-562B2F26-2437-4658-884A-DABE3F11E016Q36783519-525F40C4-C46E-48B5-B2EA-70804B77B9DDQ37181775-9DC5EEAC-C745-4FB2-9BA6-E8167918A2B9Q37275173-D3F05E33-F236-4739-B94B-8F9AE0522AD4Q37292534-7F5F9547-1CA5-4AE9-B7D8-991E73D09256Q37421261-C89B0097-2F91-4494-A0B3-345481DC4A95Q37816055-7DA34C8E-4079-45D2-B1E7-3D853A1263C7Q37827896-B7299FDC-A8D7-4E3E-B166-08760DC5B817Q38754326-52E02A73-6AE9-4A92-BB5A-764BC91AEFE5Q38909768-88073585-3529-4FBC-A202-6719373FE9F2Q39024184-B9B8ABEC-74ED-4D49-B1BD-DADF0055F43BQ39244531-04407F57-CF4F-4778-99CD-F63C4F336925Q39897686-D22A884A-57EC-4E4E-B7B3-BFC333516632Q44670045-F7756F3D-5DAF-4E2F-B6D3-59E756EB97A8Q45754958-CB324BCD-22DD-4245-8543-CB02F2AA1B55Q47285730-A495B566-CB30-47B5-9749-FAAA43EE4E6EQ47591745-2EB2C399-F153-4D16-BEC1-8C61BD8630F7Q50278381-C3D29B43-1636-4E4A-BE49-4EBC6AE0B2AEQ50310101-8B109A11-4918-4701-84A4-843B33364E87Q50586542-E06E074B-FAE5-4B87-8D25-196C38DD9300Q53673484-FB2EE9B3-F056-4157-9052-F3D196B1C1C6Q55089341-7735334C-9B27-42E7-8B35-AE74B56CEF9B
P2860
A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh
2007年學術文章
@zh-hant
name
A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.
@ast
A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.
@en
type
label
A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.
@ast
A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.
@en
prefLabel
A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.
@ast
A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.
@en
P2093
P2860
P1476
A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.
@en
P2093
Debra Skinner
Donald B Bailey
Ian Whitmarsh
P2860
P304
P356
10.1016/J.SOCSCIMED.2007.04.034
P407
P577
2007-06-11T00:00:00Z