Novel subtype of congenital partial lipodystrophy with mandibular hypoplasia, sensorineural deafness and short stature of unknown genetic origin

Những quyển sách tương tự

• A Novel Syndrome of Mandibular Hypoplasia, Deafness, and Progeroid Features Associated with Lipodystrophy, Undescended Testes, and Male Hypogonadism
  Bằng: Shastry, Savitha, et al.
  Được phát hành: (2010)
• The first Japanese patient with mandibular hypoplasia, deafness, progeroid features and lipodystrophy diagnosed via POLD1 mutation detection
  Bằng: Okada, Asami, et al.
  Được phát hành: (2017)
• A Chinese girl with mandibular hypoplasia, deafness, progeroid features, and lipodystrophy (MDPL) diagnosed via POLD1 mutation detection
  Bằng: Wang, Xiu-Wen, et al.
  Được phát hành: (2020)
• A De Novo POLD1 Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner Syndrome
  Bằng: Wang, Linda R., et al.
  Được phát hành: (2018)
• Sensorineural deafness.
  Bằng: Douek, E
  Được phát hành: (1990)