(Q43105030)

14 November 2017

Nonrandom X-chromosome inactivation in hemopoietic cells from carriers of dyskeratosis congenita (English)

1 reference

14 November 2017

Ferraris AM

1

1 reference

14 November 2017

Forni GL

series ordinal

2

1 reference

14 November 2017

Mangerini R

series ordinal

3

1 reference

14 November 2017

Gaetani GF

series ordinal

4

1 reference

14 November 2017

language of work or name

English

0 references

publication date

1 August 1997

1 reference

American Journal of Human Genetics

14 November 2017

1 reference

14 November 2017

61

1 reference

14 November 2017

2

1 reference

14 November 2017

458-461

1 reference

Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita

14 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Fine mapping of the dyskeratosis congenita locus in Xq28.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Nonrandom X-inactivation patterns in normal females: lyonization ratios vary with age.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Heritability of X chromosome--inactivation phenotype in a large family

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Dyskeratosis congenita: an inherited bone marrow failure syndrome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Dyskeratosis congenita: three additional families show linkage to a locus in Xq28.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Langerhans'-cell histiocytosis (histiocytosis X)--a clonal proliferative disease.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Genetic control of X inactivation and processes leading to X-inactivation skewing.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Expression of the gene defect in X-linked agammaglobulinemia

15 August 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9297%2807%2964075-0

Assignment of the gene for dyskeratosis congenita to Xq28

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9297%2807%2964075-0

Polyclonal origin of medullary carcinoma of the thyroid in multiple endocrine neoplasia type 2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9297%2807%2964075-0

Dyskeratosis congenita: unusual presenting features within a kindred

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9297%2807%2964075-0

Allelic exclusion of glucose-6-phosphate dehydrogenase in platelets and T lymphocytes from a Wiskott-Aldrich syndrome carrier

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9297%2807%2964075-0

"Stem cell" origin of the hematopoietic defect in dyskeratosis congenita

7 January 2021

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9311754

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S0002-9297(07)64075-0

1 reference

14 November 2017

1 reference

14 November 2017

1 reference