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The expanding genetic and clinical landscape associated with Meier-Gorlin syndrome.
Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome.
Left cerebral hemisphere and ventricular system abnormalities in a Mexican Meier Gorlin syndrome patient: widening the clinical spectrum.
Meier-Gorlin (ear-patella-short stature) syndrome: growth hormone deficiency and previously unrecognized findings.
Meier-Gorlin syndrome (ear-patella-short stature syndrome) in an Italian patient: clinical evaluation and analysis of possible candidate genes.