P gene mutations in patients with oculocutaneous albinism and findings suggestive of Hermansky-Pudlak syndrome

Samankaltaisia teoksia

• Hermansky-Pudlak syndrome and oculocutaneous albinism in Chinese children with pigmentation defects and easy bruising
  Tekijä: Bradley Power, et al.
  Julkaistu: (2019-02-01)
• Hermansky-Pudlak syndrome and oculocutaneous albinism in Chinese children with pigmentation defects and easy bruising
  Tekijä: Power, Bradley, et al.
  Julkaistu: (2019)
• Oculocutaneous albinism and bruising in two sisters--probable Hermansky-Pudlak syndrome.
  Tekijä: Ellis, J P, et al.
  Julkaistu: (1995)
• Hermansky-Pudlak Syndrome: Mutation Update
  Tekijä: Huizing, Marjan, et al.
  Julkaistu: (2020)
• Genetic Testing for Oculocutaneous Albinism Type 1 and 2 and Hermansky–Pudlak Syndrome Type 1 and 3 Mutations in Puerto Rico
  Tekijä: Santiago Borrero, Pedro J., et al.
  Julkaistu: (2006)