Pure terminal duplication of the short arm of chromosome 19 in a boy with mild microcephaly
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Cited by 8 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. A rare intrauterine onset growth retardation syndrome caused by mosaic 19p13.3 microduplication: evaluation of gh/igf- 1 axis and gh therapy response;The Turkish Journal of Pediatrics;2021
2. Nonmosaic Trisomy 19p13.3p13.2 Resulting from a Rare Unbalanced t(Y;19)(q12;p13.2) Translocation in a Patient with Pachygyria and Polymicrogyria;Cytogenetic and Genome Research;2020
3. Limited survivability of unbalanced progeny of carriers of a unique t(4;19)(p15.32;p13.3): a study in multiple generations;Molecular Cytogenetics;2017-08-04
4. Duplication of 19p13.3 in 11-Year-Old Male Patient with Dysmorphic Features and Intellectual Disability: A Review;Journal of Pediatric Genetics;2017-06-02
5. A novel immunodeficiency syndrome associated with partial trisomy 19p13;Journal of Medical Genetics;2014-01-15
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