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Keywords: Asymptomatic
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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
... of chromosome 1q are rare and associated with clinical features including growth restriction, developmental delays, and dysmorphic features. Here, we describe an asymptomatic family with an interstitial 1q31 deletion found incidentally. Case Presentation: A 42-year-old male presented with concerns...