Broad phenotypic spectrum of germ line 7p12.1 microdeletions encompassing the IKZF1 gene includes predisposition to acute lymphoblastic leukemia-Reference-Cited by-同舟云学术

Broad phenotypic spectrum of germ line 7p12.1 microdeletions encompassing the IKZF1 gene includes predisposition to acute lymphoblastic leukemia

Published:2020-11-18 Issue:2 Volume:60 Page:79-87
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes Cancer

Author:

Pastorczak Agata¹^ORCID,Hogendorf Anna²,Urbanska Zuzanna¹^ORCID,Budzynska Edyta³,Jesionek‐Kupnicka Dorota⁴,Gach Agnieszka⁵,Hawula Wanda⁵,Smigiel Robert⁶,Skiba Pawel⁷,Sasiadek Maria⁷,Lejman Monika⁸,Constatinou Maria³,Lipska‐Ziętkiewicz Beata S.⁹¹⁰^ORCID,Mlynarski Wojciech¹^ORCID

Affiliation:

1. Department of Pediatrics, Oncology and Hematology Medical University of Lodz Lodz Poland

2. Department of Pediatrics, Diabetology, Endocrinology and Nephrology Medical University of Lodz Lodz Poland

3. Department of Clinical Genetics Medical University of Lodz Lodz Poland

4. Department of Pathology, Chair of Oncology Medical University of Lodz Lodz Poland

5. Department of Medical Genetics Polish Mother's Memorial Hospital‐Research Institute Lodz Poland

6. Department of Pediatrics, Division of Propaedeutic Pediatrics and Rare Disorders Wroclaw Medical University Wroclaw Poland

7. Department of Genetics Wroclaw Medical University Wroclaw Poland

8. Laboratory of Genetic Diagnostics Medical University of Lublin Lublin Poland

9. Centre for Rare Diseases Medical University of Gdansk Gdansk Poland

10. Clinial Genetics Unit, Department of Biology and Medical Genetics Medical University of Gdansk Gdansk Poland

Funder

European Cooperation in Science and Technology

Polpharma Scientific Foundation

Publisher

Wiley

Subject

Cancer Research,Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/gcc.22914

Reference26 articles.

1. Loss of B Cells in Patients with Heterozygous Mutations in IKAROS

2. Acute lymphoblastic leukemia in a patient with Greig cephalopolysyndactyly and interstitial deletion of chromosome 7 del(7)(p11.2 p14) involving theGLI3 andZNFN1A1 genes

3. Microdeletion of 7p12.1p13, including IKZF 1 , causes intellectual impairment, overgrowth, and susceptibility to leukaemia

4. Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients

5. Genomic analysis of five chromosome 7p deletion patients with Greig cephalopolysyndactyly syndrome (GCPS)

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