https://www.selleckchem.com/products/U0126.html
BACKGROUND Two loci (CHD7 and SOX1 underlying Kallmann syndrome (KS) were discovered through clinical and genetic analysis of CHARGE and Waardenburg syndromes, conditions that include congenital anosmia caused by olfactory bulb defects (CA/OBs) and congenital hypogonadotropic hypogonadism (CHH). We hypothesized that other candidate genes for KS could be discovered by analyzing rare syndromes presenting with these signs. STUDY DESIGN, SIZE, DURATION We first investigated a family with Gorlin-Goltz syndrome (GGS) in which affected members
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