(Q54534920)

English

Identification of deletions in the btk gene allows unambiguous assessment of carrier status in families with X-linked agammaglobulinaemia.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

Identification of deletions in the btk gene allows unambiguous assessment of carrier status in families with X-linked agammaglobulinaemia. (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

1

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

5

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

author name string

A Sweatman

2

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

S A Genet

3

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

H R Middleton-Price

4

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

I Vorechovsky

6

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

D Bentley

7

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

G Fontan

8

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

T Español

9

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

G Morgan

10

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

publication date

1 July 1994

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

94

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

1

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

77-79

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

Genetic linkage analysis identifies new proximal and distal flanking markers for the X-linked agammaglobulinemia gene locus, refining its localization in Xq22

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier determination for X-linked agammaglobulinemia using X inactivation analysis of purified B cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation detection in the X-linked agammaglobulinemia gene, BTK, using single strand conformation polymorphism analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of two loci, DXS454 and DXS458, with respect to the X-linked agammaglobulinemia gene locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three dinucleotide repeat polymorphisms at the DXS178 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dinucleotide repeat polymorphism at the DXS178 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fabry disease: molecular diagnosis of hemizygotes and heterozygotes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02272846

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/8034298

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