CARRIER TESTING IN FRAGILE X SYNDROME: MENTAL RETARDATION & BIOETHICS

牙釉质发生中，牙釉质发育的个体表现出遗传异质性， 常染色体显性、X连锁和可能的常染色体隐性 遗传方式有牵连。 这些调查 确认和建立更多的遗传联系， 以及建立疾病的分子基础， 所涉及的特定基因座与表型之间的关系 可变性

Amelogenesis imperfecta appears to exhibit genetic heterogeneity, with autosomal dominant, X-linked and possible autosomal recessive modes of inheritance being implicated. These investigations are undertaken to confirm and establish additional genetic linkages as well as to establish the molecular basis of the disorder and any relationships between the specific locus(loci) involved and phenotypic variability.