Bilateral microtiaGene: MCM5
Meier-Gorlin syndrome 8 (MIM617564) is on the exclusion criteria for this panel. Associated with phenotype in OMIM, not in G2P. At least two variants reported as compound heterozygotes in one case (PMID 28198391)
Created: 17 Aug 2017, 11:57 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
?Meier-Gorlin syndrome 8 617564
MCM5 was created by sleigh
MCM5 was added to Bilateral microtiapanel. Sources: Literature