Hokkaido Univ Sch of Med
Dept of Peds
Two novel mutations of the CYP11B2 gene in a Japanese patient with aldosterone deficiency type 1
Do broad GNAS methylation defects modify the Albright's hereditary osteodystrophy phenotypes in pseudohypoparathyroidism type 1?
Two novel mutations of the thyroid peroxidase gene in two Japanese patients with congenital hypothyroidism (CH) detected by neonatal screening