Prenatal detection of genetic disorders.
作者信息
Epstein C J, Schneider E L, Conte F A, Friedman S
出版信息
Am J Hum Genet. 1972 Mar;24(2):214-26.
Abstract
摘要
相似文献
1
Prenatal detection of genetic disorders.遗传性疾病的产前检测。
Am J Hum Genet. 1972 Mar;24(2):214-26.
2
[Prenatal diagnosis in medical genetics].
Union Med Can. 1971 Nov;100(11):2213-22.
3
Prenatal diagnosis of genetic disorders: trials and tribulations.遗传性疾病的产前诊断：试验与磨难
Clin Chem. 1972 Mar;18(3):179-87.
4
Prenatal genetic diagnosis. I.产前基因诊断。一。
N Engl J Med. 1970 Dec 17;283(25):1370-81. doi: 10.1056/NEJM197012172832505.
5
Amniocentesis: a means of pre-natal diagnosis of conditions associated with severe mental subnormality.羊膜穿刺术：一种用于产前诊断与严重智力发育迟缓相关病症的方法。
Br J Psychiatry. 1971 Jan;118(542):83-6. doi: 10.1192/bjp.118.542.83.
6
The use of amniocentesis for prenatal genetic counseling.羊膜穿刺术在产前遗传咨询中的应用。
Bull N Y Acad Med. 1970 Nov;46(11):916-21.
7
Amniocentesis for prenatal genetic studies.用于产前基因研究的羊膜穿刺术。
Obstet Gynecol. 1972 Jul;40(1):104-8.
8
Prenatal genetics and cytogenetics.
J Iowa Med Soc. 1971 Sep;61(9):546-53.
9
[Possibilites and limitations in the prenatal diagnosis of genetic diseases].[遗传性疾病产前诊断的可能性与局限性]
Brux Med. 1972 Feb;52(2):109-21.
10
[Amniocentesis indications and diagnostics].
Rev Med Suisse Romande. 1974 Oct;94(10):793-802.
引用本文的文献
1
Transport and storage of amniotic fluid samples for prenatal diagnosis of metabolic diseases.
Humangenetik. 1973;20(2):175-8. doi: 10.1007/BF00284856.
2
Prenatal diagnosis of genetic disorders by amniocentesis.通过羊膜穿刺术进行遗传性疾病的产前诊断。
Calif Med. 1973 Nov;119(5):1-6.
3
The prenatal diagnosis of metabolic disorders.代谢紊乱的产前诊断。
J R Coll Physicians Lond. 1973 Apr;7(3):251-8.
4
Prenatal diagnosis and genetic counselling.产前诊断与遗传咨询。
J Clin Pathol Suppl (R Coll Pathol). 1974;8:150-5.
本文引用的文献
1
Antenatal sex determination.产前性别鉴定
Nature. 1956 Feb 18;177(4503):330. doi: 10.1038/177330a0.
2
Chromosomal problems of intrauterine diagnosis.宫内诊断的染色体问题。
Birth Defects Orig Artic Ser. 1971 Apr;7(5):10-4.
3
X-linked mental retardation without physical abnormality: Renpenning's syndrome.
Dev Med Child Neurol. 1971 Feb;13(1):71-8. doi: 10.1111/j.1469-8749.1971.tb03033.x.
4
In utero diagnosis of Niemann-Pick disease.尼曼-匹克病的宫内诊断
Am J Hum Genet. 1971 Sep;23(5):533-5.
5
Genetic counselling in Down's syndrome.唐氏综合征的遗传咨询
Hum Hered. 1970;20(5):457-64. doi: 10.1159/000152346.
6
Antenatal detection of hereditary disorders.遗传性疾病的产前检测
Pediatrics. 1968 Dec;42(6):912-8.
7
Intrauterine diagnosis and management of genetic defects.宫内遗传缺陷的诊断与处理
Am J Obstet Gynecol. 1967 Nov 15;99(6):796-807. doi: 10.1016/0002-9378(67)90395-x.
8
Chromosome analysis of human amniotic-fluid cells.
Lancet. 1966 Feb 19;1(7434):383-5. doi: 10.1016/s0140-6736(66)91387-0.
9
Prenatal genetic diagnosis (second of three parts).产前基因诊断（共三部分，第二部分）
N Engl J Med. 1970 Dec 24;283(26):1441-7. doi: 10.1056/NEJM197012242832605.
Zotero 插件