Hereditary disease and its control.
作者信息
Evans P R
出版信息
Br Med J. 1975 Jul 19;3(5976):141-4. doi: 10.1136/bmj.3.5976.141.
Abstract
摘要
相似文献
1
Hereditary disease and its control.遗传性疾病及其控制。
Br Med J. 1975 Jul 19;3(5976):141-4. doi: 10.1136/bmj.3.5976.141.
2
Prevention of hereditary disease.遗传性疾病的预防。
S Afr Med J. 1974 Jul 20;48(35):1500-6.
3
Genetic screening.基因筛查
Annu Rev Genet. 1975;9:67-89. doi: 10.1146/annurev.ge.09.120175.000435.
4
The role of screening in the prevention of inherited disease in South Africa.筛查在南非预防遗传性疾病中的作用。
S Afr Med J. 1977 Jun 4;51(23):832-7.
5
Prevention and control of genetic disease.遗传病的预防与控制。
J R Coll Physicians Lond. 1974 Jan;8(2):107-14.
6
Genetic screening legislation.基因筛查立法
Adv Hum Genet. 1975;5:319-76. doi: 10.1007/978-1-4615-9068-2_5.
7
What science can do about hereditary diseases.科学能如何应对遗传性疾病。
Fortune. 1974 Sep;90(3):148-152+.
8
It's wrong to knowingly beget defective children.故意生育有缺陷的孩子是错误的。
US Cathol. 1976 Feb;41(2):12-4.
9
[Delivery of a healthy infant following intrauterine genetic diagnosis].[宫内基因诊断后分娩出健康婴儿]
Orv Hetil. 1974 Jun 23;115(25):1455-6.
10
Prenatal diagnosis of X-linked diseases.X连锁疾病的产前诊断。
Clin Genet. 1980 Aug;18(2):147-50.
本文引用的文献
1
Children of incest.乱伦所生子女。
Pediatrics. 1967 Jul;40(1):55-62.
2
The sphingolipidoses.鞘脂贮积症
N Engl J Med. 1966 Aug 11;275(6):312-8. doi: 10.1056/NEJM196608112750606.
3
Treatment of Fabry's disease: correction of the enzymatic deficiency by renal transplantation.
J Lab Clin Med. 1971 Dec;78(6):989-90.
4
Bacterial virus gene expression in human cells.人类细胞中的细菌病毒基因表达。
Nature. 1971 Oct 8;233(5319):398-400. doi: 10.1038/233398a0.
5
Fate of protein-containing liposomes injected into rats. An approach to the treatment of storage diseases.注入大鼠体内的含蛋白质脂质体的命运。一种治疗贮积病的方法。
Eur J Biochem. 1972 Jan 21;24(3):485-91. doi: 10.1111/j.1432-1033.1972.tb19710.x.
6
Genetic divergence in relatives of PKU's: low IQ correlation among normal siblings.苯丙酮尿症亲属的基因差异：正常兄弟姐妹间智商相关性低。
Dev Psychobiol. 1974 Jul;7(4):323-30. doi: 10.1002/dev.420070409.
7
Replacement therapy for inherited enzyme deficiency. Use of purified ceramidetrihexosidase in Fabry's disease.遗传性酶缺乏的替代疗法。纯化的神经酰胺三己糖苷酶在法布里病中的应用。
N Engl J Med. 1973 Jul 5;289(1):9-14. doi: 10.1056/NEJM197307052890103.
8
Intensive plasmapheresis as a therapeutic measure in Rhesus-immunised women.强化血浆置换作为恒河猴免疫女性的一种治疗措施。
Lancet. 1970 Apr 18;1(7651):793-8. doi: 10.1016/s0140-6736(70)92406-2.
9
Association between phenylketonuria gene and rhesus, P.G.M., and Kell systems.苯丙酮尿症基因与恒河猴血型、磷酸葡萄糖变位酶及凯尔血型系统之间的关联。
Lancet. 1973 Jun 2;1(7814):1255. doi: 10.1016/s0140-6736(73)90573-4.
10
Treatment of Hurler syndrome.黏多糖贮积症I型的治疗
Lancet. 1972 Oct 21;2(7782):883. doi: 10.1016/s0140-6736(72)92257-x.
Zotero 插件