Contribution of Rare Copy Number Variants to Isolated Human Malformations-Reference-Cited by-同舟云学术

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Contribution of Rare Copy Number Variants to Isolated Human Malformations

Published:2012-10-03 Issue:10 Volume:7 Page:e45530
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Serra-Juhé Clara,Rodríguez-Santiago Benjamín,Cuscó Ivon,Vendrell Teresa,Camats Núria,Torán Núria,Pérez-Jurado Luis A.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Cited by 23 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. Identification of Extremely Rare Pathogenic CNVs by Array CGH in Saudi Children with Developmental Delay, Congenital Malformations, and Intellectual Disability;Children;2023-03-31

2. DMBX1 knockdown inhibits colorectal cancer cell proliferation and migration via down-regulating c-Myc expression;2022-09-09

3. Mixed ancestry analysis of whole-genome sequencing identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves;2021-08-10

4. Predictors of congenital anomalies among newborns in Arsi zone public hospitals, Southeast Ethiopia: a case-control study;Italian Journal of Pediatrics;2021-06-30

5. Congenital anomalies prevalence in Addis Ababa and the Amhara region, Ethiopia: a descriptive cross-sectional study;BMC Pediatrics;2019-07-11

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