A terminal 3p26.3 deletion is not associated with dysmorphic features and intellectual disability in a four-generation family
Author:
Affiliation:
1. Department of Clinical Genetics; Leiden University Medical Center; Leiden the Netherlands
2. Department of Pediatrics; Lange Land Hospital; Zoetermeer the Netherlands
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference32 articles.
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3. Subtelomeric imbalances in phenotypically normal individuals;Balikova;Hum Mutat,2007
4. Terminal 3p deletions: Phenotypic variability, chromosomal non-penetrance, or gene modification;Barber;Am J Med Genet Part A,2008
5. Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome;Cargile;Am J Med Genet,2002
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2. Cell Adhesion Molecules Involved in Neurodevelopmental Pathways Implicated in 3p-Deletion Syndrome and Autism Spectrum Disorder;Frontiers in Cellular Neuroscience;2021-01-13
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