Advances in genetics.
作者信息
Lees M M, Winter R M
机构信息
Mothercare Unit of Clinical Genetics and Fetal Medicine, Institute of Child Health, London.
出版信息
Arch Dis Child. 1996 Oct;75(4):346-50. doi: 10.1136/adc.75.4.346.
Abstract
摘要
相似文献
1
Advances in genetics.遗传学进展。
Arch Dis Child. 1996 Oct;75(4):346-50. doi: 10.1136/adc.75.4.346.
2
Advances in genetics: spiralling into trouble?遗传学进展：是否陷入困境？
Med Leg J. 2001;69(Pt 1):4-12. doi: 10.1258/rsmmlj.69.1.4.
3
Molecular genetic approaches to the analysis and diagnosis of human inherited disease: an overview.人类遗传性疾病分析与诊断的分子遗传学方法：概述
Ann Med. 1992 Feb;24(1):29-42. doi: 10.3109/07853899209164142.
4
[Genetics and immunology in medicine].[医学中的遗传学与免疫学]
Vestn Ross Akad Med Nauk. 1995(8):23-32.
5
Integration of genetics into medical practice.将遗传学融入医学实践。
Growth Horm IGF Res. 2004 Jun;14 Suppl A:S146-9. doi: 10.1016/j.ghir.2004.03.032.
6
Recent advances. Medical genetics.最新进展。医学遗传学。
BMJ. 1996 Apr 20;312(7037):1021-5. doi: 10.1136/bmj.312.7037.1021.
7
[Human genetics, today and tomorrow].[人类遗传学，现在与未来]
Monatsschr Kinderheilkd. 1990 Jun;138(6):307-15.
8
Genetics and developing countries.遗传学与发展中国家。
BMJ. 2001 Apr 28;322(7293):1006-7. doi: 10.1136/bmj.322.7293.1006.
9
Is the new genetics outpacing primary medicine?新遗传学是否发展得比初级医学更快？
Minn Med. 1992 May;75(5):18-23.
10
How will the new genetics work?新的遗传学将如何发挥作用？
Br Med J (Clin Res Ed). 1983 Jan 1;286(6358):1-2. doi: 10.1136/bmj.286.6358.1.
本文引用的文献
1
Current status of CF gene therapy.囊性纤维化基因治疗的现状。
Trends Genet. 1996 Mar;12(3):81-4. doi: 10.1016/0168-9525(96)81410-7.
2
First trimester serum screening for Down's syndrome.孕早期唐氏综合征血清筛查。
Prenat Diagn. 1995 Dec;15(13):1227-40. doi: 10.1002/pd.1970151305.
3
Clinical and molecular cytogenetic (FISH) diagnosis of Williams syndrome.威廉姆斯综合征的临床及分子细胞遗传学（荧光原位杂交）诊断
Arch Dis Child. 1996 Jan;74(1):59-61. doi: 10.1136/adc.74.1.59.
4
Clinical experience with preimplantation genetic diagnosis of cystic fibrosis (delta F508).囊性纤维化（ΔF508）植入前基因诊断的临床经验。
Prenat Diagn. 1996 Feb;16(2):137-42. doi: 10.1002/(SICI)1097-0223(199602)16:2<137::AID-PD824>3.0.CO;2-H.
5
An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p.一个位于3号染色体短臂上，易导致线粒体DNA多次缺失的常染色体基因座。
Am J Hum Genet. 1996 Apr;58(4):763-9.
6
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching.通过EST数据库搜索鉴定与果蝇突变基因同源的人类cDNA并进行图谱绘制。
Nat Genet. 1996 Jun;13(2):167-74. doi: 10.1038/ng0696-167.
7
Yeast genes and human disease.酵母基因与人类疾病。
Nature. 1996 Feb 15;379(6566):589-90. doi: 10.1038/379589a0.
8
Expanding spectrum of mitochondrial disorders.线粒体疾病谱的扩展
J Pediatr. 1996 May;128(5 Pt 1):597-9. doi: 10.1016/s0022-3476(96)80121-1.
9
Serum screening for Down's syndrome between 8 and 14 weeks of pregnancy. International Prenatal Screening Research Group.妊娠8至14周时唐氏综合征的血清筛查。国际产前筛查研究小组。
Br J Obstet Gynaecol. 1996 May;103(5):407-12. doi: 10.1111/j.1471-0528.1996.tb09765.x.
10
Somatic overgrowth associated with overexpression of insulin-like growth factor II.与胰岛素样生长因子II过表达相关的体细胞过度生长。
Nat Med. 1996 Mar;2(3):311-6. doi: 10.1038/nm0396-311.
Zotero 插件