A new MspI restriction fragment length polymorphism in the hemophilia B locus (Q45883636)

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

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2411652

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/2411652

title

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

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2411652

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/2411652

main subject

hemophilia

0 references

hemophilia B

0 references

author name string

G Camerino

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2411652

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/2411652

I Oberlé

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2411652

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/2411652

D Drayna

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2411652

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/2411652

J L Mandel

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2411652

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/2411652

publication date

1 January 1985

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2411652

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/2411652

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2411652

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/2411652

volume

71

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2411652

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/2411652

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2411652

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/2411652

page(s)

79-81

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2411652

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/2411652

cites work

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2411652

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2411652

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonrandom association of polymorphic restriction sites in the β-globin gene cluster

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2411652

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2411652

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exclusion of haemophilia B in male fetus by chorionic villus biopsy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2411652

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphic DNA markers in prenatal diagnosis of fragile X syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2411652

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2411652

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene structure of human anti-haemophilic factor IX.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2411652

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization of the human factor IX gene by molecular hybridization

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2411652

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2411652

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2411652

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00295673

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2411652

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/2411652

Dimensions Publication ID

1002944313

0 references

PubMed publication ID

2411652

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2411652

retrieved

17 December 2017

reference URL

http://europepmc.org/abstract/MED/2411652

 

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