(Q45885362)

English

De novo mutation in hemophilia A established by DNA haplotype analysis and precluding prenatal diagnosis

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

De novo mutation in hemophilia A established by DNA haplotype analysis and precluding prenatal diagnosis (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

0 references

0 references

author name string

M Delpech

1

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

N Deburgrave

2

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

M Baudis

3

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

P Maissonneuve

4

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

J M Bardin

5

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

Y Sultan

6

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

J C Kaplan

7

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

publication date

1 November 1986

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

74

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

3

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

316-317

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

Antenatal diagnosis and carrier detection of haemophilia A using factor VIII gene probe

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linked and intragenic probes for haemophilia A.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A clinically useful DNA probe closely linked to haemophilia A

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of haemophilia A by factor VIII gene analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the human factor VIII gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877941

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/2877941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

First trimester prenatal diagnosis and detection of carriers of haemophilia A using the linked DNA probe DX13.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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/2877941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemophilia A. Detection of molecular defects and of carriers by DNA analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-chromosome-specific probe DX13 for carrier detection and first trimester prenatal diagnosis in haemophilia A

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1st prenatal diagnosis of hemophilia A by direct puncture of the umbilical cord

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation analysis of hemophilia A and B

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877941

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/2877941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor VIII gene specific probe for prenatal diagnosis of haemophilia A.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00282556

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2877941

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