refine search
Authors
Locations
Journals
Publication Dates
Find concepts in Knowledge Base
Explore current query
documentsstatisticstop authorclipboard
1 documents found
1: Title: Co-occurrence of mosaic supernumerary isochromosome 18p and intermittent 2q13 deletions in a child with multiple congenital anomalies.
Authors: Jaiswal, Sushil Kumar, et.al. .
Journal: Gene, Vol. 559 (1): 94-8, 2015 .
Snippet: Moreover, 255 kbp intermittent deletion of chromosome 2q13 involving RGPD5, RGPD6, LIMS3, and LIMS3-LOC440895 was also observed.
Affiliation: Centre for Genetic Disorders, Banaras Hindu University, Varanasi, Uttar Pradesh 221005, India. Electronic address: sushil.biotech@yahoo.co.in. Department of Pediatrics, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh 221005, India. Electronic address: ashokkumar_bhu@hotmail.com. Centre for Genetic Disorders, Banaras Hindu University, Varanasi, Uttar Pradesh 221005, India. Electronic address: akhtar@bhu.ac.in. Centre for Genetic Disorders, Banaras Hindu University, Varanasi, Uttar Pradesh 221005, India. Electronic address: akrai10@gmail.com. .
Related Products: order online
Documents per page: 20 | 50 | 100