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. 1985 Aug;22(4):243–249. doi: 10.1136/jmg.22.4.243

Molecular genetics of the human X chromosome.

K E Davies
PMCID: PMC1049443  PMID: 2995673

Abstract

The human X chromosome will soon be mapped at 10 cM intervals. This will permit the localisation of any X linked disorder provided that informative families are available for linkage analysis. The location of RFLPs currently in use for clinical diagnosis is summarised. The next decade should witness the elucidation of the molecular basis of some of the more common defects, such as the muscular dystrophies and X linked mental retardation.

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Selected References

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