Interstitial 3p25.3–p26.1 deletion in a patient with intellectual disability
✍ Scribed by Angelika Riess; Ute Grasshoff; Karin Schäferhoff; Michael Bonin; Olaf Riess; Veronka Horber; Andreas Tzschach
- Book ID
- 115549395
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 208 KB
- Volume
- 158A
- Category
- Article
- ISSN
- 1552-4825
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## Abstract Deletion 3p syndrome is associated with characteristic facial features, growth failure, and mental retardation. Typically, individuals with deletion 3p syndrome have terminal deletions that result in loss of material from 3p25 to 3pter. We present a child with a clinical phenotype consi
## Abstract A partial deletion of chromosome band 2p25.3 (2pter) is a rarely described cytogenetic aberration in patients with intellectual disability (ID). Using microarrays we identified deletions of 2p25.3, sized 0.37–3.13 Mb, in three adult siblings and three unrelated patients. All patients ha