Genomic characterization of chromosome 8 pericentric trisomy-Reference-Cited by-同舟云学术

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Genomic characterization of chromosome 8 pericentric trisomy

Published:2015-05-20 Issue:7 Volume:3 Page:570-577
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Vander Pluym Juliana H.¹,O'Sullivan Julia¹,Andrew Gail²,Bolduc Francois V.¹³

Affiliation:

1. Division of Pediatric Neuroscience Stollery Children Hospital University of Alberta Edmonton Alberta Canada

2. Division of Neurodevelopmental and Neuromotor Pediatrics University of Alberta Edmonton Alberta Canada

3. Neuroscience and Mental Health Institute University of Alberta Edmonton Alberta Canada

Funder

Canadian Institutes of Health Research

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.234

Reference32 articles.

1. Array comparative genomic hybridization in global developmental delay

2. Diagnostic utility of array-based comparative genomic hybridization in a clinical setting

3. Forty four probands with an additional ?marker? chromosome

4. Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome.

5. Somatic mosaicism detected by exon-targeted, high-resolution aCGH in 10 362 consecutive cases

Cited by 5 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. Mosaic variant of trisomy on chromosome 8 (Warkany syndrome): report on a rare clinical case in a newborn boy after IVF fertilization;Meditsinskiy sovet = Medical Council;2023-07-27

2. Myelodysplastic syndrome with trisomy 8 presenting periodic fever and multiple MEFV gene variants outside exon 10: a case report;NAGOYA J MED SCI;2023

3. PLS3 whole gene deletion as a cause of X-linked osteoporosis: Clinical report with review of published PLS3 literature;Clinical Dysmorphology;2022-11-28

4. Contribution of de novo and inherited rare CNVs to very preterm birth;Journal of Medical Genetics;2020-02-12

5. 8p11 Microduplication Is Associated with Neonatal Stridor;Molecular Syndromology;2018

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