Zobrazeno 1 - 2
of 2
pro vyhledávání: '"E P, Bormann"'
Publikováno v:
Genetics and molecular research : GMR. 6(4)
Retinitis pigmentosa (RP) is a heterogeneous group of inherited retinal degeneration. This group of disorders essentially leads to blindness due to mutations in different genes. The genetic basis affected by sporadic and inherited autosomal dominant,
Publikováno v:
Brazilian dental journal. 3(1)
Three clinical cases of odontoma were detected in 2 children and 1 adolescent. The tumors were surgically removed. Clinical suspicion was based on facial deformity in one of the cases and on the absence of permanent tooth eruption in the other two. R