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1)  Basal cell nevus syndrome
基底细胞痣综合征
1.
Basal cell nevus syndrome:Report of one case and review of the literature;
基底细胞痣综合征1例报告及文献复习
2.
Basal cell nevus syndrome is a rare autosomal dominant disorder.
基底细胞痣综合征是一种罕见的常染色体显性遗传病,其致病基因为PTCH,定位于9q22。
2)  nevoid basal cell carcinoma syndrome
痣样基底细胞癌综合征
1.
A case of nevoid basal cell carcinoma syndrome family;
痣样基底细胞癌综合征家系1例
2.
Nevoid basal cell carcinoma syndrome:Report of one case and review of the literature;
痣样基底细胞癌综合征1例报告
3.
Methods PCRSSCP and DNA sequencing were used to analyze the PTCH gene mutations in 12 OKCs,including 10 sporadic and 2 nevoid basal cell carcinoma syndrome(NBCCS) associated OKC.
方法采用PCR-SSCP筛查与DNA直接测序的方法对12例OKC进行PTCH基因突变的检测,其中2例为痣样基底细胞癌综合征(NBCCS)相关OKC,10例为散发OKC。
3)  nevoid basal cell carcinoma syndrome (NBCCS)
痣样基底细胞癌综合症
4)  linear unilateral basal cell nevus (LBCN)
线状单侧基底细胞痣
5)  epidermal nevi syndrome
表皮痣综合征
6)  hemophagocytic syndrome
噬血细胞综合征
1.
Study of early experimental indexes changes on hemophagocytic syndrome;
噬血细胞综合征早期实验室指标改变研究
2.
Retrospective analysis of clinical characteristics and factors affecting prognosis of 28 children with hemophagocytic syndrome
儿童噬血细胞综合征28例临床特点和预后分析
3.
Clinical characteristics of 68 children with hemophagocytic syndrome
儿童噬血细胞综合征68例临床研究
补充资料:基底动脉偏头痛综合征


基底动脉偏头痛综合征


病名。即经前紧张性头痛综合征。详见该条。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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