Detection of polymorphisms at cytosine phosphoguanadine dinucleotides and diagnosis of haemophilia B carriers (Q45884245)

17 December 2017

title

Detection of polymorphisms at cytosine phosphoguanadine dinucleotides and diagnosis of haemophilia B carriers (English)

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17 December 2017

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2

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17 December 2017

author name string

P R Winship

series ordinal

1

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17 December 2017

M Alkan

series ordinal

3

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17 December 2017

language of work or name

English

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publication date

1 March 1989

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17 December 2017

published in

The Lancet

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17 December 2017

volume

1

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17 December 2017

issue

8639

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17 December 2017

page(s)

631-634

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17 December 2017

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

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

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Diagnosis of haemophilia B carriers using intragenic oligonucleotide probes

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7 January 2021

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

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7 January 2021

MspI polymorphic site within the factor IX gene. Localization of the site and an improved method for detection

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7 January 2021

A fraction of the mouse genome that is derived from islands of nonmethylated, CpG-rich DNA

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7 January 2021

5-Methylcytosine in eukaryotic DNA.

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7 January 2021

The effect of site-specific methylation on restriction-modification enzymes

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7 January 2021

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

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https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2992141-7

7 January 2021

The gene structure of human anti-haemophilic factor IX.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2992141-7

7 January 2021

Haemophilia B caused by a point mutation in a donor splice junction of the human factor IX gene

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https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2992141-7

7 January 2021

A simple method for DNA restriction site mapping

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7 January 2021

Recurrent mutations in haemophilia A give evidence for CpG mutation hotspots

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7 January 2021

Identification of the molecular defect in factor IX Chapel Hill: substitution of histidine for arginine at position 145.

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7 January 2021

Defective propeptide processing of blood clotting factor IX caused by mutation of arginine to glutamine at position -4.

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7 January 2021

Molecular basis of base substitution hotspots in Escherichia coli

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7 January 2021

DNA methylation and the frequency of CpG in animal DNA.

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7 January 2021

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

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7 January 2021

Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome

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7 January 2021

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

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Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).

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7 January 2021

10.1016/S0140-6736(89)92141-7

Identifiers

DOI

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17 December 2017

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17 December 2017