Micro-duplications of 1q32.1 associated with neurodevelopmental delay
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference15 articles.
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2. Congenital ocular defects associated with an abnormality of the human chromosome 1: trisomy 1q32-qter;Clark;J. Pediatr. Opthalmol. Strabismus,1994
3. Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome;Duba;J. Med. Genet.,1997
4. De novo duplication 1q32-q42: variability of phenotypic features in partial 1q trisomics;Lungarotti;J. Med. Genet.,1980
5. De novo 1q32q44 duplication and distal 1q trisomy syndrome;Nowaczyk;Am. J. Med. Genet. A,2003
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