Deletion and duplication of 15q24: Molecular mechanisms and potential modification by additional copy number variants-Reference-Cited by-同舟云学术

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Deletion and duplication of 15q24: Molecular mechanisms and potential modification by additional copy number variants

Published:2010-09 Issue:9 Volume:12 Page:573-586
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

El-Hattab Ayman W.,Zhang Feng,Maxim Rolanda,Christensen Katherine M.,Ward Jewell C.,Hines-Dowell Stacy,Scaglia Fernando,Lupski James R.,Cheung Sau Wai

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference69 articles.

Cited by 31 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. Prenatal diagnosis of a 15q24.1 microdeletion in a fetus with cerebral and urogenital abnormalities;Clinical Genetics;2024-07-16

2. The clinical value of optical genome mapping in the rapid characterization of RB1 duplication and 15q23q24.2 triplication, for more appropriate prenatal genetic counselling;Molecular Genetics & Genomic Medicine;2024-04

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

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

5. Prenatal Identification and Molecular Characterization of Two Simultaneous De Novo Interstitial Duplications of Chromosomal Regions 7p22.1p21.1 and 15q24.1;Case Reports in Genetics;2018

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