Acute lymphoblastic leukemia in a patient with Greig cephalopolysyndactyly and interstitial deletion of chromosome 7 del(7)(p11.2 p14) involving theGLI3 andZNFN1A1 genes-Reference-Cited by-同舟云学术

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

Published:2004 Issue:1 Volume:42 Page:82-86
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosom. Cancer

Author:

Mendoza-Londono Roberto,Kashork Catherine D.,Shaffer Lisa G.,Krance Robert,Plon Sharon E.

Publisher

Wiley

Subject

Cancer Research,Genetics

Reference24 articles.

1. Strike three for GLI3

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

3. Control of lymphocyte development by the Ikaros gene family

4. Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalities.

5. Variable phenotype in Greig cephalopolysyndactyly syndrome: Clinical and radiological findings in 4 independent families and 3 sporadic cases with identifiedGLI3 mutations

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review;Genes;2021-10-23

2. Broad phenotypic spectrum of germ line 7p12.1 microdeletions encompassing the IKZF1 gene includes predisposition to acute lymphoblastic leukemia;Genes, Chromosomes and Cancer;2020-11-18

3. Predisposition to childhood acute lymphoblastic leukemia caused by a constitutional translocation disrupting ETV6;Blood Advances;2019-09-13

4. Genetic Predisposition to Childhood Cancer in the Genomic Era;Annual Review of Genomics and Human Genetics;2019-08-31

5. Microdeletion of 7p12.1p13, including IKZF 1 , causes intellectual impairment, overgrowth, and susceptibility to leukaemia;British Journal of Haematology;2018-07-13