(Q52113035)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12407714%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

title

Molecular cytogenetic characterization of a 10p14 deletion that includes the DGS2 region in a patient with multiple anomalies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12407714%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12407714%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

author name string

Timm O Goecke

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12407714%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

Frank Majewski

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12407714%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

Oliver Bartsch

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12407714%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

publication date

1 November 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12407714%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics Part A

14 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12407714%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

volume

113

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12407714%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12407714%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

page(s)

207-212

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12407714%20AND%20SRC:MED&resulttype=core&format=json

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients

14 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10764

Functional evidence for the presence of tumor suppressor gene on chromosome 10p15 in human prostate cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10764

Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10764

An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10764

Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10764

DiGeorge anomaly associated with 10p deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10764

Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10764

GATA3 haplo-insufficiency causes human HDR syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10764

The transcription factor GATA-3 is necessary and sufficient for Th2 cytokine gene expression in CD4 T cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10764

A common region of 10p deleted in DiGeorge and velocardiofacial syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10764

No evidence for chromosomal microdeletions at the second DiGeorge syndrome locus on 10p near D10S585

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10764

DiGeorge anomaly and chromosome 10p deletions: one or two loci?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10764

DiGeorge anomaly with renal agenesis in infants of mothers with diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10764

21 January 2018

Identifiers

DOI

10.1002/AJMG.10764

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12407714%20AND%20SRC:MED&resulttype=core&format=json

release_f7tuk2pkovfofnle2cgju2txvq

14 December 2019

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/f7tuk2pkovfofnle2cgju2txvq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference