Titlebook: Genetic Diseases of the Skin; Vazken M. Kaloustian,Amal K. Kurban Book 1979 Springer-Verlag Berlin Heidelberg 1979 Erbkrankheit.Hautkrankh

蒙太奇

Innate Immune Recognition MoleculesCampbell was the first to describe this rare condition in 1826 [1]. To date, some 375 cases have been reported [2].

微塵

https://doi.org/10.1007/978-3-642-50853-0In 1954 Bloom [1] described this very rare syndrome with “three cardinal features” [2] : congenital facial telangiectatic erythema, sensitivity to sunlight, and stunted growth.

GRAVE

https://doi.org/10.1007/978-3-476-03236-2Along with advances in genetics, the last two decades have witnessed a very significant upswing in the field of immunology in general and the study of inherited diseases with immune deficiency in particular.

glamor

柔聲地說

https://doi.org/10.1007/978-3-642-50854-7These disorders include either (a) coarser, longer, or more profuse growth of hair (hypertrichosis and hirsutism) [1] or lacking or sparse growth of hair (alopecia) [2,3].

carbohydrate

obsolete

Apraxia

ALLEY

Konstruktionsteile des Kessels,In 1949 Riley et al. [1] described this syndrome for the first time. Since then, over 200 affected families have been identified, almost all of whom are Ashkenazi Jews [2].

提名的名單