Zobrazeno 1 - 5
of 5
pro vyhledávání: '"G C, Black"'
Publikováno v:
Ceska a slovenska oftalmologie : casopis Ceske oftalmologicke spolecnosti a Slovenske oftalmologicke spolecnosti. 67(5-6)
To describe the phenotype in an asymptomatic 64-year-old patient with family history of Best disease and to identify the disease causing variant in the BEST1 gene.Detailed ocular examination of the proband including spectral-domain optical coherence
Autor:
A E, Ridgway, S, Akhtar, F L, Munier, D F, Schorderet, H, Stewart, R, Perveen, R E, Bonshek, M T, Odenthal, M, Dixon, R, Barraquer, R, Escoto, G C, Black
Publikováno v:
Investigative ophthalmologyvisual science. 41(11)
Two mutations (R555Q and R124L) in the BIGH3 gene have been described in anterior or Bowman's layer dystrophies (CDB). The clinical, molecular, and ultrastructural findings of five families with CDB was reviewed to determine whether there is a consis
Publikováno v:
Human mutation. 15(6)
Autor:
G C, Black, A L, Ashton
Publikováno v:
Primary care. 12(3)
Preventive medicine focuses on the identification of factors that will lead to disability or disease and then the discovery of ways to eliminate or at least minimize these risk factors. In this article, the authors outline a guide for primary health
Publikováno v:
The American journal of psychiatry. 131(12)