Variant: rs387906917 

    present in Gene: CDT1
    present in Chromosome: 16
    Position on Chromosome: 88807390
    Alleles of this Variant: G/A

rs387906917 in CDT1 gene and EAR, PATELLA, SHORT STATURE SYNDROME PMID 22333897 2012 Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis.

PMID 23023959 2012 Meier-Gorlin syndrome: growth and secondary sexual development of a microcephalic primordial dwarfism disorder.

PMID 21358632 2011 Mutations in the pre-replication complex cause Meier-Gorlin syndrome.

rs387906917 in CDT1 gene and MEIER-GORLIN SYNDROME 4 PMID 21358632 2011 Mutations in the pre-replication complex cause Meier-Gorlin syndrome.

PMID 21358631 2011 Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome.