Family MRX9 revisited: further evidence for locus heterogeneity in MRX.

@article{Winnepenninckx2002FamilyMR,
  title={Family MRX9 revisited: further evidence for locus heterogeneity in MRX.},
  author={B. Winnepenninckx and V. Errijgers and E. Reyniers and P. D. De Deyn and F. Abidi and C. Schwartz and R. Kooy},
  journal={American journal of medical genetics},
  year={2002},
  volume={112 1},
  pages={
          17-22
        }
}
Nonspecific X-linked mental retardation (MRX) patients are characterized by mental retardation, without additional distinguishing features. Consequently, MRX families can only be distinguished by mapping studies; yet, due to imprecise mapping studies performed in the past, the number of genes causing MRX is debatable, and a more precise localization for families is necessary to estimate this number. MRX 9 has been mapped to the pericentromeric region Xp21-q13. We refined the mapping of the MRX9… Expand
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