Condition: Small for gestational age (disorder)


rs1554333853 in CDK13 gene and Small for gestational age (disorder) PMID 28807008 2017 Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders.

rs151344517 in LOC107985154;AFG3L2;TUBB6 gene and Small for gestational age (disorder) PMID 20725928 2010 Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias.

rs121908557 in SCN4A;LOC105371858 gene and Small for gestational age (disorder) PMID 15596759 2004 New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis.

PMID 19065518 2008 [The construction and preliminary investigation of the cell model of a novel mutation R675Q in the SCN4A gene identified in a Chinese family with normokalemic periodic paralysis].

rs1327062642 in TULP1 gene and Small for gestational age (disorder) PMID 29178942 2017 Antioxidant effect of aqueous extract of four plants with therapeutic potential on gynecological diseases; Semen persicae, Leonurus cardiaca, Hedyotis diffusa, and Curcuma zedoaria.