(Q45886848)

17 December 2017

title

The impact of prenatal diagnosis on the incidence of haemophilia in Sweden (English)

1 reference

17 December 2017

0 references

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R Ljung

1

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17 December 2017

S Kling

series ordinal

2

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17 December 2017

U Tedgird

series ordinal

3

1 reference

17 December 2017

publication date

1 July 1995

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17 December 2017

published in

Haemophilia

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17 December 2017

volume

1

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17 December 2017

issue

3

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17 December 2017

page(s)

190-193

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17 December 2017

Plasma assay of fetal factors VIIIC and IX for prenatal diagnosis of haemophilia

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1995.TB00066.X

Characterization of the human factor VIII gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1995.TB00066.X

Nucleotide sequence of the gene for human factor IX (antihemophilic factor B)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1995.TB00066.X

Sex ratio of the mutation frequencies in haemophilia A: estimation and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1995.TB00066.X

Direct estimate of the haemophilia B (factor IX deficiency) mutation rate and of the ratio of the sex-specific mutation rates in Sweden

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1995.TB00066.X

10.1111/J.1365-2516.1995.TB00066.X

21 January 2018

Identifiers

DOI

1 reference

17 December 2017

1 reference

17 December 2017