Genetic disease.
出版信息
Can Med Assoc J. 1968 Feb 24;98(8):414-6.
Abstract
摘要
相似文献
1
Genetic disease.遗传病
Can Med Assoc J. 1968 Feb 24;98(8):414-6.
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[Genetic polymorphism of drug metabolism: therapeutic implications].[药物代谢的基因多态性：治疗意义]
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The genetical background of therapy.治疗的遗传背景。
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10
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本文引用的文献
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AN ALDOSTERONE BIOSYNTHETIC DEFECT IN A SALT-LOSING DISORDER.一种失盐性疾病中的醛固酮生物合成缺陷。
J Clin Endocrinol Metab. 1964 Jul;24:669-72. doi: 10.1210/jcem-24-7-669.
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A gene locus concerned with hemolytic complement in Mus musculus.小家鼠中一个与溶血补体有关的基因位点。
Genetics. 1963 May;48(5):711-5. doi: 10.1093/genetics/48.5.711.
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Two cases of acatalasia in Switzerland.瑞士的两例过氧化氢酶缺乏症病例。
Experientia. 1961 Oct 15;17:466. doi: 10.1007/BF02158293.
4
Specificity and inheritance of antibody response: a possible steering mechanism.抗体反应的特异性与遗传性：一种可能的调控机制。
Nature. 1960 Nov 19;188:619-22. doi: 10.1038/188619a0.
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[The allotype of certain blood protein antigens].[某些血液蛋白质抗原的同种异型]
C R Hebd Seances Acad Sci. 1956 May 23;242(21):2606-8.
6
Progressive oral gangrene probably due to lack of catalase in the blood (acatalasaemia); report of nine cases.进行性口腔坏疽可能因血液中缺乏过氧化氢酶（无过氧化氢酶血症）；9例报告
Lancet. 1952 Dec 6;2(6745):1101-4. doi: 10.1016/s0140-6736(52)90939-2.
7
Allotypy and eniotypy.同种异型和个体型。
Nature. 1966 Jun 18;210(5042):1291-2. doi: 10.1038/2101291b0.
8
Growth-hormone deficiency in man: an isolated, recessively inherited defect.人类生长激素缺乏症：一种孤立的、隐性遗传缺陷。
Science. 1966 Jun 17;152(3729):1635-7. doi: 10.1126/science.152.3729.1635.
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