(Q45873298)

17 December 2017

title

Detection of a molecular defect in 40 of 44 patients with haemophilia B by PCR and denaturing gradient gel electrophoresis (English)

1 reference

17 December 2017

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Tartary M

1

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17 December 2017

Vidaud D

2

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17 December 2017

Piao Y

3

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17 December 2017

Costa JM

4

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17 December 2017

Bahnak BR

5

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17 December 2017

Fressinaud E

6

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17 December 2017

Congard B

7

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17 December 2017

Laurian Y

8

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17 December 2017

Meyer D

9

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17 December 2017

Lavergne JM

10

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17 December 2017

language of work or name

English

0 references

publication date

1 August 1993

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17 December 2017

British Journal of Haematology

published in

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17 December 2017

volume

84

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17 December 2017

issue

4

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17 December 2017

page(s)

662-669

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17 December 2017

Mutations in the catalytic domain of human coagulation factor IX: rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behavior

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1993.TB03143.X

The coagulation cascade: initiation, maintenance, and regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1993.TB03143.X

DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: correspondence with melting theory

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1993.TB03143.X

Haemophilia B: database of point mutations and short additions and deletions--third edition, 1992

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1993.TB03143.X

Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1993.TB03143.X

Key residues involved in calcium-binding motifs in EGF-like domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1993.TB03143.X

Molecular characterization of severe hemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1993.TB03143.X

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1993.TB03143.X

Nearly all single base substitutions in DNA fragments joined to a GC-clamp can be detected by denaturing gradient gel electrophoresis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1993.TB03143.X

Factor VIII gene explains all cases of haemophilia A

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1993.TB03143.X

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1993.TB03143.X

DNA sequencing with chain-terminating inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1993.TB03143.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1993.TB03143.X

10.1111/J.1365-2141.1993.TB03143.X

21 January 2018

Identifiers

DOI

1 reference

17 December 2017

PubMed ID

8217825

1 reference

17 December 2017