Abnormal Myelination in Ring Chromosome 18 Syndrome-Reference-Cited by-同舟云学术

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Abnormal Myelination in Ring Chromosome 18 Syndrome

Published:2012-01-30 Issue:8 Volume:27 Page:1042-1047
ISSN:0883-0738
Container-title:Journal of Child Neurology
language:en
Short-container-title:J Child Neurol

Author:

Benini Ruba¹,Saint-Martin Christine²³,Shevell Michael I.¹⁴,Bernard Genevieve¹⁴

Affiliation:

1. Division of Pediatric Neurology, McGill University, Montreal, Quebec, Canada

2. Department of Medical Imaging, McGill University, Montreal, Quebec, Canada

3. Division of Pediatric Radiology, McGill University, Montreal, Quebec, Canada

4. Departments of Neurology/Neurosurgery & Pediatrics, McGill University, Montreal, Quebec, Canada

Publisher

SAGE Publications

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/0883073811430268

Reference41 articles.

1. Preferential loss of the paternal alleles in the 18q- syndrome

2. Clinical and chromosomal studies of the 18q-syndrome

3. 18q deletions: Clinical, molecular, and brain MRI findings of 14 individuals

Cited by 10 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. Imaging Findings and MRI Patterns in a Cohort of 18q Chromosomal Abnormalities;American Journal of Neuroradiology;2024-05-30

2. Cerebral white matter abnormalities associated with chromosome 18q duplication;Brain and Development;2022-09

3. Genetic disorders with central nervous system white matter abnormalities: An update;Clinical Genetics;2020-10-20

4. Primary antibody deficiency associated with ring chromosome 18;LymphoSign Journal;2020-03-01

5. Brain white matter abnormalities associated with copy number variants;American Journal of Medical Genetics Part A;2019-10-17

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