Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion.
作者信息
Renwick J H, Bundey S E, Ferguson-Smith M A, Izatt M M
出版信息
J Med Genet. 1971 Dec;8(4):407-16. doi: 10.1136/jmg.8.4.407.
Abstract
摘要
相似文献
1
Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion.强直性肌营养不良症与ABH分泌位点连锁关系的确认。
J Med Genet. 1971 Dec;8(4):407-16. doi: 10.1136/jmg.8.4.407.
2
3
Prenatal prediction in myotonic dystrophy: guidelines for genetic counseling.强直性肌营养不良的产前预测：遗传咨询指南
Clin Genet. 1973;4(1):38-45. doi: 10.1111/j.1399-0004.1973.tb01120.x.
4
Genetic linkage between the loci for myotonic dystrophy and peptidase D.强直性肌营养不良症基因座与肽酶D之间的遗传连锁
Ann Hum Genet. 1983 May;47(2):117-21. doi: 10.1111/j.1469-1809.1983.tb00978.x.
5
Myotonic dystrophy: opportunities for prenatal prediction.强直性肌营养不良：产前预测的机遇
Neurology. 1975 Aug;25(8):789-91. doi: 10.1212/wnl.25.8.789.
6
Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophy.外周神经纤维瘤病（冯·雷克林豪森病）与19号染色体上与强直性肌营养不良相关的标记物的连锁分析。
J Med Genet. 1986 Feb;23(1):55-7. doi: 10.1136/jmg.23.1.55.
7
Additions to the myotonic dystrophy linkage group.强直性肌营养不良连锁群的新增内容。
Clin Genet. 1979 Jun;15(6):513-7. doi: 10.1111/j.1399-0004.1979.tb00835.x.
8
An analysis procedure illustrated on a triple linkage of use for prenatal diagnosis of myotonic dystrophy.一种用于强直性肌营养不良产前诊断的三联体连锁分析程序。
J Med Genet. 1971 Dec;8(4):399-406. doi: 10.1136/jmg.8.4.399.
9
[Eugenic significance of linkage between the gene loci for dystrophia myotonica (Steiner's disease) and ABH-secretor].强直性肌营养不良（施泰纳氏病）基因位点与ABH分泌型之间连锁的优生学意义
Schweiz Med Wochenschr. 1977 Mar 12;107(10):327-35.
10
Detection of heterozygotes for myotonic dystrophy.强直性肌营养不良杂合子的检测
Clin Genet. 1974;5(2):107-9. doi: 10.1111/j.1399-0004.1974.tb01669.x.
引用本文的文献
1
Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.使用克隆的补体3基因探针进行强直性肌营养不良与19号染色体序列的连锁分析。
J Med Genet. 1983 Aug;20(4):259-63. doi: 10.1136/jmg.20.4.259.
2
Localisation of genetic markers and orientation of the linkage group on chromosome 19.19号染色体上遗传标记的定位及连锁群的定向
Hum Genet. 1984;68(4):282-5. doi: 10.1007/BF00292584.
3
Linkage analysis of neurofibromatosis (von Recklinghausen disease).神经纤维瘤病（冯·雷克林豪森病）的连锁分析
J Med Genet. 1983 Oct;20(5):334-7. doi: 10.1136/jmg.20.5.334.
4
Structure and expression of the C3 gene.补体C3基因的结构与表达
Springer Semin Immunopathol. 1983;6(2-3):119-47. doi: 10.1007/BF00205869.
5
A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.人类次黄嘌呤磷酸核糖基转移酶基因座的三等位基因限制性片段长度多态性。
Proc Natl Acad Sci U S A. 1983 Jul;80(13):4035-9. doi: 10.1073/pnas.80.13.4035.
6
Myotonic dystrophy--early detection and genetic counselling.强直性肌营养不良——早期检测与遗传咨询
J Neurol. 1980;223(1):13-22. doi: 10.1007/BF00313136.
7
An analysis procedure illustrated on a triple linkage of use for prenatal diagnosis of myotonic dystrophy.一种用于强直性肌营养不良产前诊断的三联体连锁分析程序。
J Med Genet. 1971 Dec;8(4):399-406. doi: 10.1136/jmg.8.4.399.
8
Genetic heterogeneity for dystrophia myotonica.强直性肌营养不良的遗传异质性。
J Med Genet. 1972 Sep;9(3):311-5. doi: 10.1136/jmg.9.3.311.
9
10
Preclinical detection of dystrophia myotonica.强直性肌营养不良的临床前检测。
Br Med J. 1972 Apr 15;2(5806):124-5. doi: 10.1136/bmj.2.5806.124.
本文引用的文献
1
Estimation of linkage between the Lutheran and the Lewis blood groups.对路德血型与刘易斯血型之间连锁关系的评估。
Acta Pathol Microbiol Scand. 1951;29(3):339-44. doi: 10.1111/j.1699-0463.1951.tb00136.x.
2
Observations on the human group system Lewis.关于人类Lewis血型系统的观察
Acta Pathol Microbiol Scand. 1951;28(1):61-81. doi: 10.1111/j.1699-0463.1951.tb05004.x.
3
Dystrophia myotonica with special reference to Northern Ireland.强直性肌营养不良症，特别提及北爱尔兰地区
Ann Hum Genet. 1957 Jun;21(4):318-51. doi: 10.1111/j.1469-1809.1972.tb00203.x.
4
Genetic and biochemical aspects of human blood-group A-, B-, H-, Le-a- and Le-b-specificity.人类血型A、B、H、Le-a和Le-b特异性的遗传与生化方面
Br Med Bull. 1969 Jan;25(1):30-4. doi: 10.1093/oxfordjournals.bmb.a070666.
5
Early recognition of heterozygotes for the gene for dystrophia myotonica.强直性肌营养不良症基因杂合子的早期识别。
J Neurol Neurosurg Psychiatry. 1970 Jun;33(3):279-93. doi: 10.1136/jnnp.33.3.279.
6
An analysis procedure illustrated on a triple linkage of use for prenatal diagnosis of myotonic dystrophy.一种用于强直性肌营养不良产前诊断的三联体连锁分析程序。
J Med Genet. 1971 Dec;8(4):399-406. doi: 10.1136/jmg.8.4.399.
7
Widening the scope of antenatal diagnosis.扩大产前诊断的范围。
Lancet. 1969 Aug 16;2(7616):386. doi: 10.1016/s0140-6736(69)92738-x.
Zotero 插件