Nine de novo duplications affecting both maternal and paternal chromosomes and an inherited 15q11.2 deletion, in a patient with developmental delay-Reference-Cited by-同舟云学术

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Nine de novo duplications affecting both maternal and paternal chromosomes and an inherited 15q11.2 deletion, in a patient with developmental delay

Published:2015-04-09 Issue:6 Volume:3 Page:396-401
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Tayeh Marwan K.¹,Rocco Tracy¹,Ackley Todd¹,Ernst Leslie²,Glover Thomas¹²³,Innis Jeffrey W.¹³

Affiliation:

1. Department of Pediatrics and Communicable Diseases Division of Pediatric Genetics, Metabolism and Genomic Medicine University of Michigan Ann Arbor Michigan

2. Department of Pathology University of Michigan Ann Arbor Michigan

3. Department of Human Genetics University of Michigan Ann Arbor Michigan

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.241

Reference23 articles.

1. Complex translocation involving chromosomes Y, 1, and 3 resulting in deletion of segment 3q23----q25.

2. Complex chromosome rearrangements:Report of a new case and literature review

3. Pathogenic or not? Assessing the clinical relevance of copy number variants

4. Clinical Significance of De Novo and Inherited Copy-Number Variation

5. Mechanisms for recurrent and complex human genomic rearrangements

Cited by 1 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. Failure of NIPT to detect constitutional chromoanasynthesis involving chromosome 21 in a case of fetal hydrops—A case report;Clinical Case Reports;2019-09-30

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