Interstitial deletion of bands 11q21?22.3 in a three-year-old girl defined using fluorescence in situ hybridization on metaphase chromosomes
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference15 articles.
1. Peters’ Anomaly Associated With Partial Deletion of the Long Arm of Chromosome 11
2. Interstitial deletion of 11q.
3. Fiber-FISH: experiences and a refined protocol
4. Pseudoachondroplasia with de novo deletion [del(11)(q21q22.2)]
Cited by 12 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. Directly Transmitted 12.3-Mb Deletion with a Consistent Phenotype in the Variable 11q21q22.3 Region;Cytogenetic and Genome Research;2020
2. Incidental finding of paternal UPD15 in a child with a deletion of 11q21–q22.3, presenting with developmental delay, coloboma and characteristic dysmorphic features;Clinical Dysmorphology;2016-04
3. De novo interstitial deletion in the long arm of chromosome 11: a case report;Genetics and Molecular Research;2016
4. Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male;Molecular Cytogenetics;2015-09-17
5. Interstitial 11q deletion: genomic characterization and neuropsychiatric follow up from early infancy to adolescence and literature review;BMC Research Notes;2014-04-17
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