Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report
Author:
Publisher
S. Karger AG
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 genotype–phenotype correlation in split-hand/foot malformation type 1: further refinement of the phenotypic subregions within the 7q21.3 locus;Frontiers in Molecular Biosciences;2023-10-17
2. Gene expression patterns associated with caudal fin shape in the cichlid Lamprologus tigripictilis;Hydrobiologia;2022-11-18
3. Osteogenesis Imperfecta and Split Foot Malformation due to 7q21.2q21.3 Deletion Including COL1A2, DLX5/6 Genes: Review of the Literature;Journal of Pediatric Genetics;2021-11-02
4. Split hand/foot malformation associated with 20p12.1 deletion: A case report;European Journal of Medical Genetics;2020-04
5. Deletion 7q21.2-q22.1 in a case with split hand-split foot malformation, sensorineural hearing loss and intellectual disability: Phenotype subtypes and the correlation with genotypes;European Journal of Medical Genetics;2019-12
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