Clinical phenotype of the recurrent 1q21.1 copy-number variant-Reference-Cited by-同舟云学术

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Clinical phenotype of the recurrent 1q21.1 copy-number variant

Published:2016-04 Issue:4 Volume:18 Page:341-349
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Bernier Raphael,Steinman Kyle J.,Reilly Beau,Wallace Arianne Stevens,Sherr Elliott H.,Pojman Nicholas,Mefford Heather C.,Gerdts Jennifer,Earl Rachel,Hanson Ellen,Goin-Kochel Robin P.,Berry Leandra,Kanne Stephen,Snyder LeeAnne Green,Spence Sarah,Ramocki Melissa B.,Evans David W.,Spiro John E.,Martin Christa L.,Ledbetter David H.,Chung Wendy K.

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim201578.pdf

Reference34 articles.

Cited by 135 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

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2. Prenatal diagnosis of the recurrent 1q21.1 microdeletions in fetuses with ultrasound anomalies and review of the literature;Frontiers in Genetics;2024-08-29

3. A genetic-epigenetic interplay at 1q21.1 locus underlies CHD1L-mediated vulnerability to primary progressive multiple sclerosis;Nature Communications;2024-07-30

4. Early treatment for children with mental health problems and genetic conditions through a parenting intervention (The GAP): study protocol for a pragmatic randomized controlled trial;Trials;2024-07-20

5. A critical review of the impact of candidate copy number variants on autism spectrum disorder;Mutation Research - Reviews in Mutation Research;2024-07

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