(Q34568724)

3 August 2017

title

An intragenic deletion of the factor IX gene in a family with hemophilia B. (English)

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3 August 2017

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coagulation factor IX

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hemophilia B

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author name string

S H Chen

1

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3 August 2017

S Yoshitake

2

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3 August 2017

P F Chance

3

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3 August 2017

G L Bray

4

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3 August 2017

A R Thompson

5

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3 August 2017

C R Scott

6

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3 August 2017

K Kurachi

7

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3 August 2017

language of work or name

English

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publication date

1 December 1985

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Journal of Clinical Investigation

3 August 2017

published in

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3 August 2017

volume

76

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3 August 2017

issue

6

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3 August 2017

page(s)

2161-2164

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Isolation and characterization of a cDNA coding for human factor IX

3 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424334

Gene deletions in patients with haemophilia B and anti-factor IX antibodies

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424334

Factor IX and prothrombin in amniotic fluid and fetal plasma: constraints on prenatal diagnosis of hemophilia B and evidence of proteolysis.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424334

The gene structure of human anti-haemophilic factor IX.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424334

Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424334

Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424334

Molecular cloning of the gene for human anti-haemophilic factor IX.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424334

Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency).

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424334

Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424334

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424334

Detection of specific sequences among DNA fragments separated by gel electrophoresis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424334

Enzymatic synthesis of deoxyribonucleic acid. XXXII. Replication of duplex deoxyribonucleic acid by polymerase at a single strand break

7 July 2018

1 reference

12 December 2020

The partial thromboplastin time with kaolin. A simple screening test for first stage plasma clotting factor deficiencies

1 reference

12 December 2020

Regional localization of the human factor IX gene by molecular hybridization

1 reference

12 December 2020

Carrier detection by direct gene analysis in a family with haemophilia B (factor IX deficiency)

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI112222

1 reference

3 August 2017

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3 August 2017

1 reference