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Molecular studies of the parental origin and nature of human X isochromosomes.

作者信息

Harbison M, Hassold T, Kobryn C, Jacobs P A

机构信息

Department of Pediatrics, Cornell University Medical College, New York, NY.

出版信息

Cytogenet Cell Genet. 1988;47(4):217-22. doi: 10.1159/000132553.

DOI:10.1159/000132553
PMID:2901328
Abstract

X-chromosome restriction fragment length polymorphisms were used to determine the parental origin of the isochromosome in nine individuals with an i(Xq) or idic(Xq). We were able to specify the parental source of eight of the nine isochromosomes, with six being maternal and two paternal in origin. In two cases, one i(Xq) and one idic(Xq), we used Xq markers to determine the level of heterozygosity in the isochromosome. Each was homozygous at all tested loci, suggesting that each originated from a single X chromosome and not from an exchange of material between two X's.

摘要

相似文献

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Molecular studies of the parental origin and nature of human X isochromosomes.
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Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.与人类X染色体等臂染色体相关的断点的分子定义:对形成机制的启示
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Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.
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A molecular study of X isochromosomes: parental origin, centromeric structure, and mechanisms of formation.X等臂染色体的分子研究:亲本来源、着丝粒结构及形成机制。
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