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Keywords: 1q deletion
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Journal Articles
A Familial Case of 1q31.2q32.2 Deletion with No Phenotypic Presentation
Available to PurchaseSubject Area:
Genetics
Journal:
Cytogenetic and Genome Research
Cytogenet Genome Res 23–30.
Published Online: 26 February 2025
... to the development of genotype-phenotype interpretation and to decrease the uncertainty of care recommendations for patients and their families. 1q deletion CDC73 Asymptomatic Hereditary Established Facts Mutations in 1q3 region often result in developmental disorders. Novel Insights...