(Q34416691)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11673406%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

review article

1 reference

title

Human diseases with underlying defects in chromatin structure and modification (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11673406%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11673406%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

W Bickmore

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11673406%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

publication date

1 October 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11673406%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

published in

Human Molecular Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11673406%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

volume

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11673406%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11673406%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

page(s)

2233-2242

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11673406%20AND%20SRC:MED&resulttype=core&format=json

Genetic variation in ICF syndrome: evidence for genetic heterogeneity

13 November 2019

cites work

1 reference

5 October 2024

https://opencitations.net/index/api/v1/citations/10.1002/1098-1004(200012)16:6%3C509::AID-HUMU8%3E3.0.CO;2-V

Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant.

1 reference

5 October 2024

https://opencitations.net/index/api/v1/citations/10.1093/HMG/9.18.2575

The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome

1 reference

5 October 2024

https://opencitations.net/index/api/v1/citations/10.1073/PNAS.96.25.14412

Localization of the ICF syndrome to chromosome 20 by homozygosity mapping

1 reference

5 October 2024

https://opencitations.net/index/api/v1/citations/10.1086/302021

Identifiers

DOI

10.1093/HMG/10.20.2233

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11673406%20AND%20SRC:MED&resulttype=core&format=json

release_ftgqiz3e5regbet6lhol2gee7m

13 November 2019

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ftgqiz3e5regbet6lhol2gee7m

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11673406%20AND%20SRC:MED&resulttype=core&format=json