Re: Savtchenko et al. (1988): "Embryonic Expression of the Human 40-kD Keratin: Evidence from a Processed Pseudogene Sequence".
作者信息
Boklage C E
出版信息
Am J Hum Genet. 1989 Apr;44(4):590-1.
Abstract
摘要
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本文引用的文献
1
Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features.弗里德赖希共济失调：对90个家庭的临床与遗传学研究，分析早期诊断标准及临床特征的家族内聚集情况。
Brain. 1981 Sep;104(3):589-620. doi: 10.1093/brain/104.3.589.
2
Strategies for multilocus linkage analysis in humans.人类多位点连锁分析策略。
Proc Natl Acad Sci U S A. 1984 Jun;81(11):3443-6. doi: 10.1073/pnas.81.11.3443.
3
Recessive ataxia in Acadians and "Cajuns".
Can J Neurol Sci. 1984 Nov;11(4 Suppl):526-33. doi: 10.1017/s0317167100034995.
4
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。
Anal Biochem. 1983 Jul 1;132(1):6-13. doi: 10.1016/0003-2697(83)90418-9.
5
The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers.位于4号染色体上的三个限制性片段长度多态性相对于已知遗传标记的位置。
Hum Genet. 1984;68(2):154-8. doi: 10.1007/BF00279306.
6
Mapping of mutation causing Friedreich's ataxia to human chromosome 9.导致弗里德赖希共济失调的突变基因定位到人类9号染色体。
Nature. 1988 Jul 21;334(6179):248-50. doi: 10.1038/334248a0.
7
Isolation and mapping of a polymorphic DNA sequence pMCT112 on chromosome 9q (D9S15).9号染色体q臂上多态性DNA序列pMCT112（D9S15）的分离与定位
Nucleic Acids Res. 1987 Dec 23;15(24):10614. doi: 10.1093/nar/15.24.10614-a.
8
Embryonic expression of the human 40-kD keratin: evidence from a processed pseudogene sequence.人类40-kD角蛋白的胚胎表达：来自一个加工假基因序列的证据。
Am J Hum Genet. 1988 Nov;43(5):630-7.
9
Detection of specific sequences among DNA fragments separated by gel electrophoresis.在通过凝胶电泳分离的DNA片段中检测特定序列。
J Mol Biol. 1975 Nov 5;98(3):503-17. doi: 10.1016/s0022-2836(75)80083-0.
10
Clinical description and roentgenologic evaluation of patients with Friedreich's ataxia.弗里德赖希共济失调患者的临床描述与放射学评估
Can J Neurol Sci. 1976 Nov;3(4):279-86. doi: 10.1017/s0317167100025464.
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