Interstitial microdeletion of chromosome 1p in two siblings
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference9 articles.
1. A large deletion of chromosome no. 1 (46,XY,1?--).
2. Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1.
3. Uniparental isodisomy resulting from 46,XX,i(1p),i(1q) in a woman with short stature, ptosis, micro/retrognathia, myopathy, deafness, and sterility
4. Paternal Uniparental Disomy for Chromosome 1 Revealed by Molecular Analysis of a Patient with Pycnodysostosis
5. Deletion of chromosome 1p: a short review
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