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- 因子X(jué)III缺乏癥factor XIII deficiency
- 遺傳性凝血因子X(jué)III缺陷癥分子機制的研究Molecular mechanisms of two novel mutations of factor XIII gene resulting in hereditary coagulation deficiency
- 漢族人群凝血因子X(jué)III Val34Leu多態(tài)性與動(dòng)脈血栓性疾病的關(guān)系Association between polymorphism of coagulation factor XIII Val34Leu and ischemi c arterial thrombotic diseases in Han population
- 癥obstruction of bowels
- 凝血因子Ⅶ缺乏癥coagulation factor Ⅶ dificiacy
- G-CSF治療白血病化療不同階段發(fā)生的粒細胞缺乏癥療效觀(guān)察The observation of the effect of G-CSF on agranulocytosis in different chemotheraphy of acute leukemia
- 鐵缺乏癥早期early iron-deficiency anemia
- G-6-PD缺乏癥G-6-PD deficiency
- 五種微量元素缺乏癥防治制劑對肉仔雞血液甲狀腺素水平的影響Effect of the pharmaceutical preparations to prevent and cure trace elements deficiency symptom upon levels of thyroid hormones in blood of chickens
- 四氫生物喋呤缺乏癥治療前后神經(jīng)系統表現及其腦白質(zhì)病變分析Clinical manifestations and cerebral white matter changes in children with tetrahydrobiopterin deficiency before and after treatment
- 因子VII缺乏癥factor VII deficiency
- 20-裂解酶缺乏癥20-lyase deficiency
- 此外,兒童碘缺乏癥造成身體和認知發(fā)育障礙以及甲狀腺機能減退。In addition, iodine deficiency in children is responsible for disorders in physical and cognitive development, and hypothyroidism.
- 先天性因子Ⅹ缺乏癥congenital factor Ⅹ deficiency
- 蛋白質(zhì)缺乏癥[營(yíng)養不良protein malnutrition | kwashiorkor
- 先天性因子Ⅻ缺乏癥Hageman factor deficiency
- 尿苷酸合酶缺乏癥deficiency of uridine monophophate synthase
- 遺傳性因子Ⅴ缺乏癥hereditary deficiency of factor Ⅴ
- 遺傳性因子Ⅶ缺乏癥hereditary deficiency of factor Ⅶ; hereditary factor Ⅶ deficiency
- 四氫生物喋呤缺乏癥Tetrahydrob/opterin deficiency