(Q34295249)

English

ICF syndrome (immunodeficiency, centromeric instability and facial anomalies): investigation of heterochromatin abnormalities and review of clinical outcome

scientific article

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

1 reference

Europe PubMed Central

ICF syndrome (immunodeficiency, centromeric instability and facial anomalies): investigation of heterochromatin abnormalities and review of clinical outcome (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

author name string

Brown DC

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Grace E

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Sumner AT

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Edmunds AT

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Ellis PM

5

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

publication date

1 October 1995

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

96

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

411-416

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

ICF syndrome. Immunodeficiency, chromosomal centromere instability, facial anomalies. Case report and literature review

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A direct demonstration of somatically paired heterochromatin of human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ICF syndrome: a new case and review of the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragility of the centromeric region of chromosome 1 associated with combined immunodeficiency in siblings. A recessively inherited entity?

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Centromeric instability of chromosomes 1, 9, and 16 associated with combined immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Centromeric instability of chromosomes 1, 9 and 16 with variable immune deficiency. Support of a new syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Scanning electron microscopy of mammalian chromosomes from prophase to telophase

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variable immunodeficiency with abnormal condensation of the heterochromatin of chromosomes 1, 9, and 16

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ICF syndrome with variable expression in sibs

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Centromeric instability of chromosomes 1 and 16 with variable immune deficiency: a new syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7557962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00191798

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34295249&oldid=2196472991"