Mutation rates in humans. II. Sporadic mutation-specific rates and rate of detrimental human mutations inferred from hemophilia B. (Q34146302)

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English	Mutation rates in humans. II. Sporadic mutation-specific rates and rate of detrimental human mutations inferred from hemophilia B.	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Mutation rates in humans. II. Sporadic mutation-specific rates and rate of detrimental human mutations inferred from hemophilia B. (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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author name string

F Giannelli

1

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Europe PubMed Central

PubMed publication ID

31 July 2017

T Anagnostopoulos

2

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31 July 2017

P M Green

3

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Europe PubMed Central

PubMed publication ID

31 July 2017

language of work or name

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publication date

1 December 1999

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Europe PubMed Central

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31 July 2017

American Journal of Human Genetics

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Europe PubMed Central

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31 July 2017

65

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Europe PubMed Central

PubMed publication ID

31 July 2017

6

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Europe PubMed Central

PubMed publication ID

31 July 2017

1580-1587

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Mutation rates in humans. I. Overall and sex-specific rates obtained from a population study of hemophilia B.

1 reference

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5 July 2018

DNA variation in a 5-Mb region of the X chromosome and estimates of sex-specific/type-specific mutation rates

1 reference

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5 July 2018

High genomic deleterious mutation rates in hominids

1 reference

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Molecular Biology Database List

1 reference

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5 July 2018

Rates of spontaneous mutation

1 reference

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5 July 2018

Haemophilia B: database of point mutations and short additions and deletions--eighth edition

1 reference

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5 July 2018

Male-driven evolution of DNA sequences in birds

1 reference

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The high spontaneous mutation rate: is it a health risk?

1 reference

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Haemophilia B: database of point mutations and short additions and deletions, 7th edition

1 reference

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The factor IX gene as a model for analysis of human germline mutations: an update

1 reference

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Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctions

1 reference

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5 July 2018

Male-driven evolution of DNA sequences

1 reference

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

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How much do we know about spontaneous human mutation rates?

1 reference

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5 July 2018

Germ-line origins of mutation in families with hemophilia B: the sex ratio varies with the type of mutation

1 reference

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5 July 2018

Mutations of the APC (adenomatous polyposis coli) gene

1 reference

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Australopithecus ramidus, a new species of early hominid from Aramis, Ethiopia

1 reference

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Searching for the 1 in 2,400,000: a review of dystrophin gene point mutations

1 reference

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Biological basis of germline mutation: comparisons of spontaneous germline mutation rates among drosophila, mouse, and human

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Sequence variation of the human Y chromosome

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DNA methylation and the frequency of CpG in animal DNA.

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Male-driven molecular evolution: a model and nucleotide sequence analysis

1 reference

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Functionally important regions of the factor IX gene have a low rate of polymorphism and a high rate of mutation in the dinucleotide CpG.

1 reference

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Haemophilia B: database of point mutations and short additions and deletions

1 reference

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The incidence and distribution of CpG----TpG transitions in the coagulation factor IX gene. A fresh look at CpG mutational hotspots

1 reference

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The odds of losing at genetic roulette

1 reference

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28 October 2018

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1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

ResearchGate publication ID

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