Warning: The NCBI web site requires JavaScript to function. more...
An official website of the United States government
The .gov means it's official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.
The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.
MOCS2 - Retinoblastomas with loss of heterozygosity at chromosome 16q
GEO DataSets Gene Profile neighbors Chromosome neighbors Homologene neighbors
ISCA1 - Retinoblastomas with loss of heterozygosity at chromosome 16q
VPS13A - Retinoblastomas with loss of heterozygosity at chromosome 16q
EPS15 - Retinoblastomas with loss of heterozygosity at chromosome 16q
RIOK3 - Retinoblastomas with loss of heterozygosity at chromosome 16q
ANGPT4 - Retinoblastomas with loss of heterozygosity at chromosome 16q
NLRX1 - Retinoblastomas with loss of heterozygosity at chromosome 16q
ANXA7 - Retinoblastomas with loss of heterozygosity at chromosome 16q
IFT57 - Retinoblastomas with loss of heterozygosity at chromosome 16q
STXBP3 - Retinoblastomas with loss of heterozygosity at chromosome 16q
CHD5 - Retinoblastomas with loss of heterozygosity at chromosome 16q
TM2D1 - Retinoblastomas with loss of heterozygosity at chromosome 16q
SEC62 - Retinoblastomas with loss of heterozygosity at chromosome 16q
PAFAH2 - Retinoblastomas with loss of heterozygosity at chromosome 16q
NME6 - Retinoblastomas with loss of heterozygosity at chromosome 16q
SIRT3 - Retinoblastomas with loss of heterozygosity at chromosome 16q
ZMYM6 - Retinoblastomas with loss of heterozygosity at chromosome 16q
TMF1 - Retinoblastomas with loss of heterozygosity at chromosome 16q
CACTIN - Retinoblastomas with loss of heterozygosity at chromosome 16q
TRIM52 - Retinoblastomas with loss of heterozygosity at chromosome 16q
Filters: Manage Filters
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on