(Q43449433)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21906047%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

title

A novel deletion in ZBTB24 in a Lebanese family with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2 (English)

1 reference

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12 February 2020

0 references

13

1 reference

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12 February 2020

author name string

E Chouery

1

1 reference

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12 February 2020

J Abou-Ghoch

2

1 reference

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12 February 2020

S Corbani

3

1 reference

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12 February 2020

N El Ali

4

1 reference

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12 February 2020

R Korban

5

1 reference

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12 February 2020

N Salem

6

1 reference

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12 February 2020

C Castro

7

1 reference

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12 February 2020

S Klayme

8

1 reference

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12 February 2020

M Azoury-Abou Rjeily

9

1 reference

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12 February 2020

R Khoury-Matar

10

1 reference

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12 February 2020

G Debo

11

1 reference

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12 February 2020

M Germanos-Haddad

12

1 reference

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12 February 2020

G Lefranc

14

1 reference

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12 February 2020

A Mégarbané

15

1 reference

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12 February 2020

publication date

5 October 2011

1 reference

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12 February 2020

1 reference

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12 February 2020

volume

82

1 reference

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12 February 2020

issue

5

1 reference

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12 February 2020

page(s)

489-493

1 reference

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Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome)

12 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01783.X

Altered intra-nuclear organisation of heterochromatin and genes in ICF syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01783.X

Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01783.X

ICF, an immunodeficiency syndrome: DNA methyltransferase 3B involvement, chromosome anomalies, and gene dysregulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01783.X

Heterochromatic genes undergo epigenetic changes and escape silencing in immunodeficiency, centromeric instability, facial anomalies (ICF) syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01783.X

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01783.X

Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01783.X

A simple and efficient non-organic procedure for the isolation of genomic DNA from blood

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01783.X

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01783.X

Genetic variation in ICF syndrome: evidence for genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01783.X

Bone morphogenetic protein-2 induces expression of murine zinc finger transcription factor ZNF450

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01783.X

10.1111/J.1399-0004.2011.01783.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21906047%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

1 reference