(Q35199097)

7 August 2017

Population genetics of coagulant factor IX: frequencies of two DNA polymorphisms in five ethnic groups (English)

1 reference

7 August 2017

1 reference

D B Lubahn

1

1 reference

7 August 2017

S T Lord

2

1 reference

7 August 2017

J Bosco

3

1 reference

7 August 2017

J Kirshtein

4

1 reference

7 August 2017

O J Jeffries

5

1 reference

7 August 2017

N Parker

6

1 reference

7 August 2017

C Levtzow

7

1 reference

7 August 2017

L M Silverman

8

1 reference

7 August 2017

J B Graham

9

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 June 1987

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

40

1 reference

7 August 2017

527-536

1 reference

7 August 2017

6

1 reference

Isolation and characterization of a cDNA coding for human factor IX

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

Isolation of a human anti-haemophilic factor IX cDNA clone using a unique 52-base synthetic oligonucleotide probe deduced from the amino acid sequence of bovine factor IX.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

The gene structure of human anti-haemophilic factor IX.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

Isolation and characterization of human factor IX cDNA: identification of Taq I polymorphism and regional assignment

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

Caucasian Genes in American Negroes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

Evidence for a prevalent dimorphism in the activation peptide of human coagulation factor IX.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

Factor IXAlabama: a point mutation in a clotting protein results in hemophilia B.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

Use of a BamHI polymorphism in the factor IX gene for the determination of hemophilia B carrier status

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

Application of molecular genetics to prenatal diagnosis and carrier detection in the hemophilias: some limitations

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

Intragenic Factor IX restriction site polymorphism in hemophilia B variants

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

A new MspI restriction fragment length polymorphism in the hemophilia B locus

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

Detection of specific sequences among DNA fragments separated by gel electrophoresis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684156

26 September 2018

Identifiers

PMCID

1684156

1 reference

7 August 2017

1 reference