Ring chromosome 2 in a child with growth failure and few congenital abnormalities
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference5 articles.
1. Three cases of ring chromosome 2, one derived from a paternal 2/6 translocation
2. : Personal communication, 1980.
Cited by 14 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. Ring Chromosome 2;Human Ring Chromosomes;2024
2. Clinico-radiological and molecular characterization of a child with ring chromosome 2 presenting growth failure, microcephaly, kidney and brain malformations;Molecular Cytogenetics;2015-03-05
3. 35-Year Follow-Up of a Case of Ring Chromosome 2: Array-CGH Analysis and Literature Review of the Ring Syndrome;Cytogenetic and Genome Research;2015
4. Ring 2 chromosome associated with failure to thrive, microcephaly and dysmorphic facial features;Gene;2013-10
5. Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization;Gene;2013-04
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