H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency

Ítems similars

• Longitudinal Growth of the Short Bones of the Hand in a Girl with Pseudohypoparathyroidism Type Ia
  per: Nagasaki, Keisuke, et al.
  Publicat: (2007)
• The Levels of Serum Low-Density Lipoprotein Cholesterol Using Direct Measurement in Healthy Japanese School Children
  per: Ogawa, Yohei, et al.
  Publicat: (2004)
• The Relationship between Preheparin Lipoprotein Lipase and Metabolic Derangements in Obese Japanese Children
  per: Abe, Yuki, et al.
  Publicat: (2011)
• Different Skeletal Phenotypes in a Mother and Two Daughters with Short Stature Homeobox-Containing Haploinsufficiency
  per: Nagasaki, Keisuke, et al.
  Publicat: (2007)
• Two Cases of Pseudohypoparathyroidism Type Ia in Duozygotic Twins with Different Phenotypes
  per: Nagasaki, Keisuke, et al.
  Publicat: (2005)