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A possible mutation of a fluorescence polymorphism.

J A Robinson·K E Buckton·H J Evans
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Abstract

The segregation of the Q-band polymorphisms in 32 families have been studied. From 90 matings in these families, there were a total of 208 offspring. In one of these offspring it could be shown that there had been a change of a fluorescent polymorphism, resulting in the loss of fluorescent intensity in the satellite of a chromosome 21. The origin of such a 'mutation' and a consideration of mutation rates is discussed.

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Chromosomes, Human, 21-22 and YDNADNA, SatelliteFluorescenceHumansKaryotypingMutationPolymorphism, GeneticStaining and LabelingJournal Article

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BibTeXRIS

J A Robinson, K E Buckton, H J Evans. 1978. A possible mutation of a fluorescence polymorphism.. https://doi.org/10.1111/j.1469-1809.1978.tb01899.x

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