(Q36415035)

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A DNA marker closely linked to the factor IX (haemophilia B) gene

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Europe PubMed Central

PubMed publication ID

14 August 2017

A DNA marker closely linked to the factor IX (haemophilia B) gene (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

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coagulation factor IX

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author name string

L Mulligan

1

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

J J Holden

2

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

B N White

3

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

publication date

1 April 1987

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Europe PubMed Central

PubMed publication ID

14 August 2017

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Europe PubMed Central

PubMed publication ID

14 August 2017

75

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Europe PubMed Central

PubMed publication ID

14 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

381-383

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq13

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic linkage map of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphic DNA marker genetically linked to Huntington's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implications

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A computer program for linkage analysis of general human pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization of 18 human X-linked DNA sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recombination between genes and closely linked polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of haemophilia B carriers using intragenic oligonucleotide probes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probe

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene structure of human anti-haemophilic factor IX.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2883108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00284113

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

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