Hemophilia B (Christmas disease) variants and carrier detection analyzed by DNA probes (Q34567824)

3 August 2017

Hemophilia B (Christmas disease) variants and carrier detection analyzed by DNA probes (English)

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3 August 2017

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Poon MC

1

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3 August 2017

Chui DH

2

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3 August 2017

Patterson M

3

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3 August 2017

Starozik DM

4

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3 August 2017

Dimnik LS

5

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3 August 2017

Hoar DI

6

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3 August 2017

language of work or name

English

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publication date

1 April 1987

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Journal of Clinical Investigation

3 August 2017

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3 August 2017

79

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3 August 2017

4

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3 August 2017

1204-1209

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Isolation and characterization of a cDNA coding for human factor IX

3 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

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=424311

The consumers' views of genetic counseling of hemophilia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

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.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

A DNA sequence analysis package for the IBM personal computer.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

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=424311

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

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=424311

Exclusion of haemophilia B in male fetus by chorionic villus biopsy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

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=424311

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=424311

Fibrinogen Cleveland II. An abnormal fibrinogen with defective release of fibrinopeptide A.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

Application of an intragenic genomic probe to genetic counselling for haemophilia B in the west of Scotland

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

The genetic linkage map of the human X chromosome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

Gene deletion in an Italian haemophilia B subject

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

Evidence for a prevalent dimorphism in the activation peptide of human coagulation 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=424311

Structure, function, and molecular defects of 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=424311

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

An intragenic deletion of the factor IX gene in a family with hemophilia 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=424311

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

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=424311

Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

Detection and sequence of mutations in the factor VIII gene of haemophiliacs

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

Intragenic Factor IX restriction site polymorphism in hemophilia B variants

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

A new MspI restriction fragment length polymorphism in the 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=424311

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=424311

Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424311

Quantitative estimation of proteins by electrophoresis in agarose gel containing antibodies

7 July 2018

1 reference

12 December 2020

Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

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12 December 2020

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

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12 December 2020

Improved direct molecular diagnosis and rapid fetal sexing

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12 December 2020

Identifiers

DOI

10.1172/JCI112938

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3 August 2017

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3 August 2017

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