(Q36496230)

14 August 2017

A place for genetic uncertainty: parents valuing an unknown in the meaning of disease (English)

1 reference

14 August 2017

2

Arlene M Davis

1 reference

14 August 2017

Ian Whitmarsh

1

1 reference

14 August 2017

Debra Skinner

series ordinal

3

1 reference

14 August 2017

Donald B Bailey

series ordinal

4

1 reference

14 August 2017

language of work or name

English

0 references

publication date

11 June 2007

1 reference

Social Science and Medicine

14 August 2017

1 reference

14 August 2017

65

1 reference

14 August 2017

6

1 reference

14 August 2017

1082-1093

1 reference

Experiencing the genetic body: parents' encounters with pediatric clinical genetics

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

A qualitative investigation of changes in the belief systems of families of children with autism or Down syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

The best experts: the narratives of those who have a genetic condition

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Systems analysis of stress and positive perceptions in mothers and fathers of pre-school children with autism

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Illnesses you have to fight to get: facts as forces in uncertain, emergent illnesses

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Nursing leadership in genomics for health and society

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

30 September 2017

Klinefelter's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Newborn screening for fragile X syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Back pain and the resolution of diagnostic uncertainty in illness narratives

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Disclosure, confidentiality, and families: Experiences and attitudes of those with genetic versus nongenetic medical conditions

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Emplotting children's lives: developmental delay vs. disability

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Health supervision for children with Turner syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

The fragile X premutation: into the phenotypic fold

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

FMR1 and the fragile X syndrome: human genome epidemiology review

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Advances in research on the fragile X syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Intrauterine diagnosis of sex chromosome aneuploidy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Mothers of children with Down syndrome reflect on their postnatal support

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Producing genetic knowledge and citizenship through the Internet: mothers, pediatric genetics, and cybermedicine

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Living without labels: the interactional management of diagnostic uncertainty in the genetic counselling clinic.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Health professionals, their medical interventions and uncertainty: a study focusing on women at midlife.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

'I just want permission to be ill': towards a sociology of medically unexplained symptoms.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Dysmorphology and the spectacle of the clinic

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

On the proliferation of bioethics sub-disciplines: do we really need "genethics" and "neuroethics"?

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Mothers and models of disability

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Ascertainment bias in Turner syndrome: new insights from girls who were diagnosed incidentally in prenatal life

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Mothering children who have disabilities: a Bourdieusian interpretation of maternal practices

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Klinefelter syndrome: expanding the phenotype and identifying new research directions

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

"Genetic exceptionalism" in medicine: clarifying the differences between genetic and nongenetic tests

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Discovering fragile X syndrome: family experiences and perceptions.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Family experiences and factors associated with the diagnosis of fragile X syndrome.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Autistic behavior in young boys with fragile X syndrome.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Early developmental trajectories of males with fragile X syndrome.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Health professionals' reports of information given to parents following the prenatal diagnosis of sex chromosome anomalies and outcomes of pregnancies: a pilot study

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2267724

Predictive genetic testing and the making of the pre-symptomatic person: Prognostic moralities amongst Huntington's-affected families

4 December 2018

1 reference

12 December 2020

Quest, chaos and restitution: living with chronic fatigue syndrome/myalgic encephalomyelitis

1 reference

12 December 2020

Ruling in and ruling out: Implications of molecular genetic diagnoses for disease classification

1 reference

12 December 2020

Early treatment with GH alone in Turner syndrome: prepubertal catch-up growth and waning effect

1 reference

12 December 2020

Dilemmas in fetal medicine: premature application of technology or responding to women's choice?

1 reference

12 December 2020

Genetic counseling for sex chromosome abnormalities

1 reference

12 December 2020

1 reference

12 December 2020

From "reducing" to "coping with" uncertainty: reconceptualizing the central challenge in breast self-exams

1 reference

12 December 2020

To tell or not to tell: barriers and facilitators in family communication about genetic risk

1 reference

12 December 2020

10.1016/J.SOCSCIMED.2007.04.034

Identifiers

DOI

1 reference

14 August 2017

1 reference

14 August 2017

PubMed publication ID

17561324

1 reference