(Q39323888)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18266093%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

title

Impact of a genetic diagnosis of a mitochondrial disorder 5-17 years after the death of an affected child (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18266093%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18266093%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

David Thorburn

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18266093%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

author name string

M Sahhar

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18266093%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

S A Metcalfe

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18266093%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

publication date

12 February 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18266093%20AND%20SRC:MED&resulttype=core&format=json

Journal of Genetic Counseling

2 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18266093%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

volume

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18266093%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18266093%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

page(s)

261-273

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18266093%20AND%20SRC:MED&resulttype=core&format=json

Life is never the same: childhood cancer narratives.

2 January 2020

cites work

1 reference

12 December 2020

The duty to recontact: attitudes of genetics service providers.

1 reference

12 December 2020

The emergence of an ethical duty to disclose genetic research results: international perspectives

1 reference

12 December 2020

Facilitating family communication about predictive genetic testing: probands' perceptions

1 reference

12 December 2020

When you care enough to do your very best: genetic counselor experiences of compassion fatigue.

1 reference

12 December 2020

Bereaved parents’ experience of research participation

1 reference

12 December 2020

Taking a narrative approach to grief research: finding meaning in stories

1 reference

12 December 2020

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

1 reference

12 December 2020

Does research into sensitive areas do harm? Experiences of research participation after a child's diagnosis with Ewing's sarcoma

1 reference

12 December 2020

Leigh syndrome: clinical features and biochemical and DNA abnormalities.

1 reference

12 December 2020

Diagnostic criteria for respiratory chain disorders in adults and children.

1 reference

12 December 2020

Newly diagnosed childhood diabetes: a psychosocial transition for parents?

1 reference

12 December 2020

Mitochondrial disorders: prevalence, myths and advances.

1 reference

12 December 2020

Progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher syndrome): a personal review

1 reference

12 December 2020

Ethical, legal, and practical concerns about recontacting patients to inform them of new information: the case in medical genetics

1 reference

12 December 2020

Biochemical and molecular diagnosis of mitochondrial respiratory chain disorders.

1 reference

12 December 2020

Views of female breast cancer patients who donated biologic samples regarding storage and use of samples for genetic research.

1 reference

12 December 2020

Disclosing individual genetic results to research participants

1 reference

12 December 2020

Mitochondrial disorders: genetics, counseling, prenatal diagnosis and reproductive options.

1 reference

12 December 2020

Patient preferences regarding recontact by cancer genetics clinicians

1 reference

12 December 2020

Duty to re-contact: a study of families at risk for Fragile X.

1 reference

12 December 2020

How does the mode of inheritance of a genetic condition influence families? A study of guilt, blame, stigma, and understanding of inheritance and reproductive risks in families with X-linked and autosomal recessive diseases

1 reference

12 December 2020

Transmission of mitochondrial DNA disorders: possibilities for the future.

1 reference

12 December 2020

Minimum birth prevalence of mitochondrial respiratory chain disorders in children

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

POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion

1 reference

12 December 2020

Disclosure of genetics research results after the death of the patient participant: a qualitative study of the impact on relatives.

1 reference

12 December 2020

10.1007/S10897-007-9145-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18266093%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

1 reference