Application of an intragenic genomic probe to genetic counselling for haemophilia B in the west of Scotland (Q33672234)

28 July 2017

title

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

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28 July 2017

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Connor JM

1

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28 July 2017

Pettigrew AF

2

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28 July 2017

Hann IM

3

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28 July 2017

Forbes CD

4

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28 July 2017

Lowe GD

5

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28 July 2017

Affara NA

6

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28 July 2017

language of work or name

English

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publication date

1 December 1985

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

22

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28 July 2017

issue

6

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28 July 2017

page(s)

441-446

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Prenatal diagnosis of hemophilia B by an immunoradiometric assay of factor IX.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

Utility and efficiency of linked marker genes for genetic counseling. III. Proportion of informative families under linkage disequilibrium

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

The gene structure of human anti-haemophilic factor IX.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

Population genetics of C4 with the use of complementary DNA probes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

Detection of specific sequences among DNA fragments separated by gel electrophoresis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

Hemophilia B: characterization of genetic variants and detection of carriers

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

Detection of carriers of haemophilia B

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

Immunological Heterogeneity of Haemophilia B: a Multicentre Study of 98 Kindreds

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

Attitudes of Haemophilia carrier to fetoscopy and amniocentesis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

The inheritance of Christmas factor

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049503

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

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4078877

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1049503

1 reference

28 July 2017

1 reference