Myelodysplastic syndrome in a child with 15q24 deletion syndrome-Reference-Cited by-同舟云学术

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Myelodysplastic syndrome in a child with 15q24 deletion syndrome

Published:2011-12-02 Issue:2 Volume:158A Page:412-416
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Narumi Yoko,Shiohara Masaaki,Wakui Keiko,Hama Asahito,Kojima Seiji,Yoshikawa Kentaro,Amano Yoshiro,Kosho Tomoki,Fukushima Yoshimitsu

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.34395/fullpdf

Reference17 articles.

1. Genotype-phenotype correlation in four 15q24 deleted patients identified by array-CGH;Andrieux;Am J Med Genet Part A,2009

2. A report of three patients with an interstitial deletion of chromosome 15q24;Cushman;Am J Med Genet Part A,2005

3. Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping;El-Hattab;Hum Genet,2009

4. Deletion and duplication of 15q24: Molecular mechanisms and potential modification by additional copy number variants;El-Hattab;Genet Med,2010

Cited by 7 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. Coexistence of urogenital malformations in a female fetus with de novo 15q24 microdeletion and a literature review;Molecular Genetics & Genomic Medicine;2020-05-13

2. Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 15q24 microdeletion;Taiwanese Journal of Obstetrics and Gynecology;2020-05

3. Refining critical regions in 15q24 microdeletion syndrome pertaining to autism;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2020-01-18

4. NEIL1 is a candidate gene associated with common variable immunodeficiency in a patient with a chromosome 15q24 deletion;Clinical Immunology;2017-03

5. A Novel Case of 15q24 Microdeletion Syndrome Detected by MLPA in a Chinese Family;Clinical Laboratory;2017

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