(Q34522720)

2 August 2017

title

Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism (English)

1 reference

2 August 2017

S P Kwan

1

1 reference

2 August 2017

L Kunkel

2

1 reference

2 August 2017

G Bruns

3

1 reference

2 August 2017

R J Wedgwood

4

1 reference

2 August 2017

S Latt

5

1 reference

2 August 2017

F S Rosen

6

1 reference

2 August 2017

language of work or name

English

0 references

publication date

1 February 1986

1 reference

Journal of Clinical Investigation

2 August 2017

published in

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2 August 2017

volume

77

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2 August 2017

issue

2

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2 August 2017

page(s)

649-652

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2 August 2017

cites work

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1 reference

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Regional localization on the human X of DNA segments cloned from flow sorted chromosomes

7 July 2018

1 reference

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Structure and Expression of a Complementary DNA for the Nuclear Coded Precursor of Human Mitochondrial Ornithine Transcarbamylase

7 July 2018

1 reference

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A strategy to reveal high-frequency RFLPs along the human X chromosome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423409

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423409

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423409

Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423409

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

7 July 2018

1 reference

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The Primary Immunodeficiencies

7 July 2018

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Defective B cell function associated with inherited interstitial deletion of the short arm of the X chromosome

7 July 2018

1 reference

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Isolation and DNA sequence of a full-length cDNA clone for human X chromosome-encoded phosphoglycerate kinase

7 July 2018

1 reference

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Identification and characterization of subpopulations of lymphocytes in human peripheral blood after fractionation on discontinuous gradients of albumin. The cellular defect in X-linked agammaglobulinemia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423409

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423409

An RFLP detecting single copy X-chromosome fragment, dic56, from Xp22-Xpter [HGM8 assignment no. DXS 143].

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423409

Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423409

X-linked agammaglobulinemia: an analysis of 96 patients

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423409

Detection of specific sequences among DNA fragments separated by gel electrophoresis

7 July 2018

1 reference

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B lymphocyte precursors in human bone marrow: an analysis of normal individuals and patients with antibody-deficiency states

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423409

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423409

Interstitial deletion in the "critical region" of the long arm of the X chromosome in a mentally retarded boy and his normal mother.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423409

Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423409

Inherited interstitial del(Xp) with minimal clinical consequences: with a note on the location of genes controlling phenotypic features

27 October 2018

1 reference

12 December 2020

Immunodeficiency associated with a deletion in the short arm of the X-chromosome

1 reference

12 December 2020

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

12 December 2020

Primary immunodeficiency diseases. Report prepared for the WHO by a scientific group on immunodeficiency

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI112351

1 reference

2 August 2017

1 reference

2 August 2017

1 reference