(Q45879165)

17 December 2017

title

Screening for mutations in the gene encoding factor IX (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1357229

17 September 2022

author name string

L. R. Nielsen

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1357229

17 September 2022

M. Schwartz

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1357229

17 September 2022

E. Scheibel

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1357229

17 September 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1357229

17 September 2022

publication date

1 January 1992

1 reference

17 December 2017

Journal of Inherited Metabolic Disease

published in

1 reference

17 December 2017

volume

15

1 reference

17 December 2017

issue

3

1 reference

17 December 2017

page(s)

339-341

1 reference

17 December 2017

https://scigraph.springernature.com/pub.10.1007/bf02435971

exact match

0 references

cites work

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

1 reference

12 December 2020

Molecular pathology of haemophilia B

1 reference

12 December 2020

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

12 December 2020

Detection and localization of single base changes by denaturing gradient gel electrophoresis

1 reference

12 December 2020

Direct detection of point mutations by mismatch analysis: application to haemophilia B.

1 reference

12 December 2020

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

1 reference

12 December 2020

Haemophilia B mutations in a complete Swedish population sample: a test of new strategy for the genetic counselling of diseases with high mutational heterogeneity

1 reference

12 December 2020

Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02435971

1 reference

17 December 2017

Dimensions Publication ID

0 references

1 reference

17 December 2017