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Chromosome heteromorphism analysis in cases of disputed paternity.

作者信息

Olson S B, Magenis R E, Rowe S I, Lovrien E W

出版信息

Am J Med Genet. 1983 May;15(1):47-55. doi: 10.1002/ajmg.1320150106.

DOI:10.1002/ajmg.1320150106
PMID:6574701
Abstract

Blood test results, using standard procedures, failed to exclude the alleged father as the biological father of a child in a case of disputed paternity. Using 21 different systems, the probability of exclusion for the man was 98.19%, and the probability of paternity was only 93.90% with a paternity index of 15.48. Chromosome heteromorphisms of all three individuals were studied. By comparison of fluorescent markers of chromosomes 13, 14, 15, 21, and 22, the child was shown to inherit one homologue of each of these chromosomes from the mother, but none were like the heteromorphisms of the alleged father. This excluded him as the biological father.

摘要

相似文献

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引用本文的文献

1
Investigation of human chromosome polymorphisms by scanning electron microscopy.通过扫描电子显微镜对人类染色体多态性的研究。
J Med Genet. 1985 Feb;22(1):16-23. doi: 10.1136/jmg.22.1.16.
2
Human chromosome variation: the discriminatory power of Q-band heteromorphism (variant) analysis in distinguishing between individuals, with specific application to cases of questionable paternity.人类染色体变异:Q带异态性(变异)分析在个体识别中的鉴别力,特别应用于亲权存疑的案例。
Am J Hum Genet. 1986 Feb;38(2):235-52.