搜索结果: 1-4 共查到“基础医学 anemia”相关记录4条 . 查询时间(0.027 秒)
Yale scientists edit gene mutations in inherited form of anemia
Yale scientists edit gene mutations inherited form anemia
2016/11/4
A Yale-led research team used a new gene editing strategy to correct mutations that cause thalassemia, a form of anemia. Their gene editing technique provided corrections to the mutations and alleviat...
Cytogenetic and Phenotypic Findings in Turkish Patients With Fanconi's Anemia
Fanconi's Anemia Mitomycin-C Diepoxybutane Chromosome breakage
2009/7/2
Fanconi's anemia is an autosomal recessive disorder with manifestation of chromosomal instability inducible by alkylating agents. Since 1989 we studied 85 patients with suspected Fanconi's anemia (FA)...
Differentiation of Fanconi and Aplastic Anemia Using Chromosomal Breakage Test in Southern Iran
Fanconi anemia Aplastic anemia Southern Iran
2015/9/15
Background: Fanconi anemia (FA) is a chromosomal breakage disorder characterized by familial aplastic anemia (AA), various congenital anomalies, and a characteristic chromosomal response to clastogeni...
THIAMINE–RESPONSIVE MEGALOBLASTIC ANEMIA,SENSORINEURAL DEAFNESS AND DIABETES MELLITUS
Refractory anemia thiamine responsive
2010/4/2
The syndrome of diabetes mellitus, sensorineural deafness and megaloblastic anemia dose not result from thiamine deficiency. The previous reported patients had no sign of beriberi, had normal nutritio...