(Q45888697)

English

A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probes

scientific article published in February 1986

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Statements

scholarly article

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3455922

A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probes (English)

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3455922

0 references

0 references

author name string

S Gilgenkrantz

1

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3455922

M E Briquel

2

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3455922

J L Mandel

3

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3455922

I Oberle

4

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3455922

publication date

1 February 1986

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3455922

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3455922

72

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3455922

2

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3455922

157-159

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3455922

https://scigraph.springernature.com/pub.10.1007/bf00283936

0 references

The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3455922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haemophilia A in a girl with deletion of a part of the long arm of one X chromosome (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/3455922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haemophilia ‘A’in a 46,X,i(Xq) Female

1 reference

https://pubmed.ncbi.nlm.nih.gov/3455922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variant of factor IX deficiency in female with 45, X Turner's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3455922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemophilia B in a phenotypically normal girl with XX (ring) XO mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/3455922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/3455922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemophilia A in a Phenotypically Normal Female with XX/XO Mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/3455922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00283936

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3455922

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3455922

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