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JCRPE.5080
JCRPE.5080
http://dx.doi.org/10.4274/JCRPE.5080
One novel 2.43Kb deletion and one single nucleotide mutation of the INSR gene in a Chinese neonate with Rabson-Mendenhall syndrome.
P356
Q50224234-C37C4CFE-B6DD-4456-9D86-C6AF7FEEFEE2
P356
JCRPE.5080
http://dx.doi.org/10.4274/JCRPE.5080