The spectrum of 4q- syndrome illustrated by a case series
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference23 articles.
1. A de novo 4q34 interstitial deletion of at least 9.3 Mb with no discernible phenotypic effect;Bateman;Am. J. Med. Genet. A,2010
2. Bilateral optic disc swelling in the 4q34 deletion syndrome;Connell;J. AAPOS,2007
3. Telomere healing following DNA polymerase arrest-induced breakages is likely the main mechanism generating chromosome 4p terminal deletions;Hannes;Hum. Mutat.,2010
4. Del(4q) syndrome;Hennekam,2010
5. T. Huang, Personal, communication, 2011.
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2. Identification of a novel isolated 4q35.2 microdeletion in a Chinese pediatric patient using chromosomal microarray analysis: a case report and literature review;Molecular Cytogenetics;2023-08-02
3. Impact of genetic structural variants in factor XI deficiency: identification, accurate characterization, and inferred mechanism by long-read sequencing;Journal of Thrombosis and Haemostasis;2023-07
4. Chromosome 4q deletion syndrome: 4q13.3-q21.23 deletion syndrome with mental retardation, congenital heart disease: a case report and literature review;2023-03-07
5. 4q interstitial and terminal deletion: clinical features comparison in two unrelated children;AIMS Medical Science;2023
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