(Q24599498)

1

Annelien Bredenoord

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Guido de Wert

6

Guido de Wert

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Guido Pennings

3

Guido Pennings

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Wybo Dondorp

2

Wybo Dondorp

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author name string

Christine de Die-Smulders

European Journal of Human Genetics

4

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language of work or name

English

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publication date

December 2009

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published in

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volume

17

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issue

12

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page(s)

1550-9

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cites work

Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

ESHRE PGD consortium data collection VII: cycles from January to December 2004 with pregnancy follow-up to October 2005.

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Dealing with uncertainties: ethics of prenatal diagnosis and preimplantation genetic diagnosis to prevent mitochondrial disorders

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Birth after transfer of frozen-thawed vitrified biopsied blastocysts

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

ESHRE Task Force on Ethics and Law 12: oocyte donation for non-reproductive purposes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Oocyte donation for stem cell research.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Approaches to the treatment of mitochondrial diseases

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Why test children for adult-onset genetic diseases?

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Inheritance of mitochondrial disorders

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Creating and sacrificing embryos for stem cells.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

International ethical guidelines for biomedical research involving human subjects.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Segregation of mitochondrial DNA (mtDNA) in human oocytes and in animal models of mtDNA disease: clinical implications.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Is there a case in favour of predictive genetic testing in young children?

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Random genetic drift determines the level of mutant mtDNA in human primary oocytes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Towards reliable prenatal diagnosis of mtDNA point mutations: studies of nt8993 mutations in oocytes, fetal tissues, children and adults

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue- or age-related variation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Skewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

Preimplantation genetic diagnosis: patients' experiences and attitudes.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987024

PGD to reduce reproductive risk: the case of mitochondrial DNA disorders.

30 May 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

Measuring the welfare of the child: in search of the appropriate evaluation principle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

Amplification of DNA sequences in polar bodies from human oocytes for diagnosis of mitochondrial disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

Prospect of preimplantation genetic diagnosis for heritable mitochondrial DNA diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

Maternally inherited Leigh syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

MELAS and MERRF. The relationship between maternal mutation load and the frequency of clinically affected offspring.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

Coming soon to your clinic: patient-friendly ART.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

Diagnostic efficiency, embryonic development and clinical outcome after the biopsy of one or two blastomeres for preimplantation genetic diagnosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

A mild treatment strategy for in-vitro fertilisation: a randomised non-inferiority trial.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

Cryopreservation of biopsied embryos at the blastocyst stage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

Clinical trials in children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

Removal of 2 cells from cleavage stage embryos is likely to reduce the efficacy of chromosomal tests that are used to enhance implantation rates

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

Patterns of ovarian response to gonadotropin stimulation in female carriers of balanced translocation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.88

Minimal risk in pediatric research

21 January 2018

1 reference

12 December 2020

Prenatal diagnosis by amniocentesis and chorionic villus biopsy of mtDNA mutation 8993T > G

1 reference

12 December 2020

Clinical application of preimplantation genetic diagnosis

1 reference

12 December 2020

74th ENMC international workshop: mitochondrial diseases 19-20 november 1999, Naarden, the netherlands

1 reference

12 December 2020

Very low levels of the mtDNA A3243G mutation associated with mitochondrial dysfunction in vivo

1 reference

12 December 2020

Detection of MELAS A3243G point mutation in muscle, blood and hair follicles

1 reference

12 December 2020

What are the trade-offs between one-cell and two-cell biopsies of preimplantation embryos?

1 reference

12 December 2020

Identifiers

DOI

10.1038/EJHG.2009.88

1 reference

Dimensions Publication ID

1047713126

0 references

1 reference

1 reference

PubMed publication ID

19471315

1 reference