Sasaki Ayako | 山形大学医学部小児科学

スポンサーリンク

概要

関連著者

もっと見る

著作論文

Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese
De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : unequal sister chromatid exchange during paternal gametogenesis
Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene : The common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese
Congenital Central Hypoventilation Syndrome : A Novel Mutation of the RET Gene in an Isolated Case
Sudden Infant Death Syndrome Is Not Associated with the Mutation of PHOX2B Gene, a Major Causative Gene of Congenital Central Hypoventilation Syndrome
Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome
Polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : rs17884724:A>C is associated with 7-alanine expansion

スポンサーリンク