Molecular characterisation of a 3.5 Mb interstitial 14q deletion in a child with several phenotypic anomalies
Author:
Publisher
BMJ
Subject
Genetics(clinical),Genetics
Cited by 22 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. Goyal-Naqvi Syndrome (Concurrent Trisomy 10p and Terminal 14q Deletion): A Review of the Literature;Cureus;2021-07-26
2. Core Competencies in Cancer Genomics for Healthcare Professionals: Results From a Systematic Literature Review and a Delphi Process;Journal of Cancer Education;2021-01-13
3. Functional characterization of a candidate tumor suppressor gene, Mirror Image Polydactyly 1 , in nasopharyngeal carcinoma;International Journal of Cancer;2020-05-15
4. Partial trisomy 9 (9pter->9q22.1) and partial monosomy 14 (14pter>14q11.2) due to paternal translocation t(9;14)(q22.1;q11.2) in a case of Dysmorphic features;Intractable & Rare Diseases Research;2019-02-28
5. Whole exome sequencing identifies a novel 5 Mb deletion at 14q12 region in a patient with global developmental delay, microcephaly and seizures;Gene;2018-10
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