(Q52087310)

English

Acute lymphoblastic leukemia in a patient with Greig cephalopolysyndactyly and interstitial deletion of chromosome 7 del(7)(p11.2 p14) involving the GLI3 and ZNFN1A1 genes.

scientific article published in January 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

Acute lymphoblastic leukemia in a patient with Greig cephalopolysyndactyly and interstitial deletion of chromosome 7 del(7)(p11.2 p14) involving the GLI3 and ZNFN1A1 genes. (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

lymphoblastic leukemia

1 reference

based on heuristic

inferred from title

Roberto Mendoza-Londono

1

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

author name string

Catherine D Kashork

2

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

Lisa G Shaffer

3

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

Robert Krance

4

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

Sharon E Plon

5

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

publication date

1 January 2005

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

Genes, Chromosomes and Cancer

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

42

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

1

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

82-86

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

Strike three for GLI3.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Six cases of 7p deletion: Clinical, cytogenetic, and molecular studies

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Control of lymphocyte development by the Ikaros gene family

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

The Ikaros gene is required for the development of all lymphoid lineages

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of Ikaros isoforms in patients with acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Lymphoma- and leukemia-associated chromosomal translocations in healthy individuals

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Importance of using comparative genomic hybridization to improve detection of chromosomal changes in childhood acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical and molecular delineation of the Greig cephalopolysyndactyly contiguous gene deletion syndrome and its distinction from acrocallosal syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Atypical chronic myelogenous leukemia in a patient with trisomy 8 mosaicism syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterization of deletions of chromosome 7 short arm occurring as primary karyotypic anomaly in acute myeloid leukaemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Ikaros expression in human hematopoietic lineages

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Ikaros, Aiolos and Helios: transcription regulators and lymphoid malignancies

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Constitutional and acquired trisomy 8

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of aberrantly spliced oncogenic ikaros isoforms in childhood acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of dominant-negative and mutant isoforms of the antileukemic transcription factor Ikaros in infant acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of the Ikaros gene family in childhood acute lymphoblastic leukaemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Constitutional trisomy 8 and myelodysplasia: report of a case and review of the literature.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20100

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.20100

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15390181

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