mtDNA point mutations are present at various levels of heteroplasmy in human oocytes (Q50639726)

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scientific article published on 26 January 2007

Language	Label	Description	Also known as
English	mtDNA point mutations are present at various levels of heteroplasmy in human oocytes	scientific article published on 26 January 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

mtDNA point mutations are present at various levels of heteroplasmy in human oocytes (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

1 reference

based on heuristic

inferred from title

6

object named as

Joep Geraedts

0 references

John C. M. Dumoulin

4

object named as

John Dumoulin

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

Patrick F. Chinnery

3

object named as

Patrick Chinnery

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

2

object named as

Mike Gerards

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

author name string

Lorraine Jacobs

1

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

Ireneaus de Coo

5

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

Joep Geraedts

6

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

Hubert Smeets

7

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

publication date

26 January 2007

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

Molecular Human Reproduction

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

13

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

3

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

149-154

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients

1 reference

12 August 2022

https://opencitations.net/index/coci/api/v1/citations/10.1097/01.GIM.0000237782.94878.05

Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups

1 reference

10 September 2024

https://opencitations.net/index/api/v1/citations/10.1086/339933

A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissues.

1 reference

9 November 2024

https://opencitations.net/index/api/v1/citations/10.1023/A:1005357506614

Mitochondrial disorders: prevalence, myths and advances.

1 reference

9 November 2024

https://opencitations.net/index/api/v1/citations/10.1023/B:BOLI.0000031098.41409.55

Identifiers

10.1093/MOLEHR/GAL112

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/17259224

ResearchGate publication ID

0 references

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