期刊文献+

多指(趾)家系疾病相关基因排除性定位分析 被引量:7

Exclusive mapping on polydactyly with markers on chromosomes 7 and 2 in a Chinese kindred
原文传递
导出
摘要 目的 定位一个常染色体显性遗传多指(趾)家系中的疾病相关基因。方法 采用已经报道的7号染色体上7个微卫星DNA标记及2号染色体上1个微卫星标记对该家系进行连锁分析。结果 7号染色体上7个位点的Z值均小于1,与该家系致病基因不连锁;2号染色体上的1个位点与致病基因明显不连锁。结论 该家系的致病基因很可能是一个新基因座。 Objective This study was aimed at mapping polydactyly related genes in a Chinese kindred.Methods Linkage analysis was performed using 7 markers on chromosome 7 and 1 marker on chromosome 2. Results\ Pairwise linkage analysis showed no linkage between the markers and polydactyly related gene in the kindred.Conclusion\ The polydactyly related gene in this kindred may be located on a new locus.
出处 《中华医学遗传学杂志》 CAS CSCD 北大核心 2000年第1期6-9,共4页 Chinese Journal of Medical Genetics
基金 "8 63"基金资助项目!Z1 9 0 1 0 4 0 1
关键词 排除性定位分析 多趾定系疾病 相关基因 polydactyly a Chinese kindred exclusive mapping
  • 相关文献

参考文献9

二级参考文献75

  • 1王殿珍,廖建梅,许爱华.1例肾移植术后对硝普钠耐受并氰化物中毒患者护理[J].第三军医大学学报,2006,28(9):895-895. 被引量:2
  • 2郭鼎,王洪波,张贯石,鲁赫鸣,孙启富,钟岩,魏春丽.血和肝脏检材保存条件对氰化物浓度的影响[J].中国法医学杂志,1996,11(4):211-213. 被引量:1
  • 3格鲁什科 Я M.工业废水中有害无机化合物[M].北京:化学工业出版社,1984..
  • 4黄光照.法医毒理学.北京:人民卫生出版社,1992.88-92.
  • 5国家药典委员会编.临床用药须知[M].北京:人民卫生出版社,2005:60
  • 6Hall VA,Guest JM.Sodium nitroprusside-induced cyanide intoxication and prevention with sodium thiosulfate prophylaxis[J].Am J Crit Care,1992,1(2):19-25.
  • 7Page IH,Corcoran AC,Dustan HP,et al.Cardiovascular action of sodium nitroprusside in animals and hypertensive patients[J].Circulation,1955,11(2):188-198.
  • 8Patel CB,Laboy V,Venus B,et al.Use of sodium nitroprusside in post-coronary bypass surgery.Aplea for conservatism[J].Chest,1986,89(5):663-667.
  • 9From The Food and Drag Administration.New labeling for sodium nitroprusside emphasized risk of cyanide toxity[J].JAMA,1991,265(7):847.
  • 10McEvoy GK.American Hospital Formulary Service Drug Information1998[M].Bethesda,MD:American Society of Health System Pharmacists,1998:1529-1532.

共引文献116

同被引文献130

  • 1徐建国,徐峰.轴后多指(趾)畸形一家系19例[J].中华医学遗传学杂志,2005,22(1):114-114. 被引量:3
  • 2曾溢滔.血红蛋白疾病的诊断和治疗[J].中华血液学杂志,1996,17(8):393-394. 被引量:36
  • 3McKusickVA.人类孟德尔遗传(第ll版)[M].北京:北京医科大学中国协和医科大学联合出版社,1996,12..
  • 4Bosse K, Betz RC, Lee YA. Localization of a gene for syndactyly type 1 to chromosome 2q34-q36. Am J Hum Genet,2000,67 :495-497.
  • 5Gladwin A,Donnai D,Metcalfe K, et al. Localization of a gene for oculodentodigital syndrome to human chromosome 6Cl22- q24 Hum Molec Genet ,1997 ,6 ; 123-127.
  • 6Zhao H, Tian Y, Breedveld G, et al. Postaxial polydactyly type A/B (PAP-A/B) is linked to chromosome 19p13. 1-13. 2 in a Chinese kindred. Eur J Hum Genet,2002,10 : 162-166.
  • 7Goodman R, Mundlos S, Muragaki Y, Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract. Proc Natl Acad Sci U S A, 1997, 94 : 7458-7463.
  • 8Radhakrishna U, Blouin JL, MehenniH, et al. Mapping one form of autosormal dominant postaxial polydactyly type A to chromosome 7plS-qll. 23 by linkage analysis. Am J Hum Genet,1997,60 :597-604.
  • 9Tsukurov O, Boehmer A, Flynn J. A complex bilateral polysyndactyly disease locus maps to chromosome 7q36. Nat Genet,1994,6 : 282-286.
  • 10Vortamp A, Gessler M, Grzesehik KH, et al, GLI3 zine-finger gene interrupted by transloeatlon in Greig syndrome families.Nature,1991,352 : 539-540.

引证文献7

二级引证文献31

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部