(Q52090390)

English

Linkage and recombination between fragile X-linked mental retardation and the factor IX gene

scientific article published in January 1985

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/3967889

Linkage and recombination between fragile X-linked mental retardation and the factor IX gene (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/3967889

author name string

S T Warren

1

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/3967889

T W Glover

2

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/3967889

R L Davidson

3

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/3967889

P Jagadeeswaran

4

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/3967889

publication date

1 January 1985

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/3967889

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/3967889

69

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/3967889

1

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/3967889

44-46

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/3967889

The marker (X) syndrome: a cytogenetic and genetic analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3967889

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition

1 reference

https://pubmed.ncbi.nlm.nih.gov/3967889

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/3967889

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/3967889

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequential tests for the detection of linkage

1 reference

https://pubmed.ncbi.nlm.nih.gov/3967889

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3967889

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/3967889

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/3967889

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marker (X)-Linked Mental Retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/3967889

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis in man.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3967889

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of human factor IX cDNA: identification of Taq I polymorphism and regional assignment

1 reference

https://pubmed.ncbi.nlm.nih.gov/3967889

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of the marker (X) (q28) in lymphoblastoid cell lines

1 reference

https://pubmed.ncbi.nlm.nih.gov/3967889

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation: a study of 7 families

1 reference

https://pubmed.ncbi.nlm.nih.gov/3967889

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male

1 reference

https://pubmed.ncbi.nlm.nih.gov/3967889

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/3967889

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00295528

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/3967889

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/3967889

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