(Q45885122)

English

Molecular studies of haemophilia B in Sweden. Identification of patients with total deletion of the factor IX gene and without inhibitory antibodies

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scholarly article

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/2848757

Molecular studies of haemophilia B in Sweden. Identification of patients with total deletion of the factor IX gene and without inhibitory antibodies (English)

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/2848757

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coagulation factor IX

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author name string

C Wadelius

1

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/2848757

M Blombäck

2

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/2848757

U Pettersson

3

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/2848757

publication date

1 December 1988

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/2848757

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/2848757

81

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/2848757

13-17

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/2848757

1

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/2848757

https://scigraph.springernature.com/pub.10.1007/bf00283721

0 references

Cytogenetic evidence concerning possible transplacental transfer of leukocytes in pregnant women

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemophilia B with inhibitor: molecular analysis of the subtotal deletion of the factor IX gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the mcf.2 transforming sequence to the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

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/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RFLP for linkage analysis of fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene deletion in an Italian haemophilia B subject

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inhibitory effect of ethidium bromide on mitotic chromosome condensation and its application to high-resolution chromosome banding

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

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/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PRODUCTION OF IMMUNE SERA TO AN ANTIHAEMOPHILIC FACTOR PREPARATION IN RABBITS TOLERANT TO FIBRINOGEN

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An intragenic deletion of the factor IX gene in a family with hemophilia B.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of a cDNA coding for human factor IX

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cause of the 'inhibitor' phenotype in the haemophilias

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

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/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

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/2848757

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/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New Giemsa method for the differential staining of sister chromatids

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26?qter

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Large scale physical mapping in the q27 region of the human X chromosome: the coagulation factor IX gene and the mcf.2 transforming sequence are separated by at most 270 kilobase pairs and are surrounded by several 'HTF islands'.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2848757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00283721

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/2848757

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/2848757

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