ASYMMETRY OF CHROMOSOME NUMBER 1 PAIR IN THREE GENERATIONS OF A PHENOTYPICALLY NORMAL FAMILY

Author:

Ying Kuang-Lin,Ives Elizabeth J.

Abstract

A family is reported in which 6 of the 15 members studied carry a greatly lengthened #1 chromosome. This has segregated in three generations without phenotypic effect.Blood grouping provides evidence in favour of linkage of the Duffy locus and #1 chromosome.Autoradiographic studies demonstrate that DNA replication in the extended region of the marker chromosome occurs late in the majority of cells but early in a small proportion of cells in each of the three individuals thus studied. Possible explanations discussed include environmental modifications in culture technique, an unstable replication pattern in the extended region, and the chance that somatic crossing over of homologues allows a shift of a hypothetical "genetic inactivation centre" from one chromosome to the corresponding region of its homologue.

Publisher

Canadian Science Publishing

Subject

Cell Biology,Plant Science,Genetics

Cited by 39 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Heterochromatic Variations and Pregnancy Losses in Humans;International Journal of Human Genetics;2011-09

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3. A 60-Year Tale of Spots, Maps, and Genes;Annual Review of Genomics and Human Genetics;2006-09-01

4. Plates;Atlas of Human Chromosome Heteromorphisms;2004

5. The origins of human gene mapping;Genomics;1987-11

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