XLMR genes: update 1998.

@article{Lubs1999XLMRGU,
  title={XLMR genes: update 1998.},
  author={HerbertA. Lubs and Pietro Chiurazzi and J. Fernando Arena and Charles Walsh Schwartz and Lisbeth Tranebjaerg and Giovanni Neri},
  journal={American journal of medical genetics},
  year={1999},
  volume={83 4},
  pages={
          237-47
        }
}
Since the Seventh Fragile X and XLMR Mental Retardation (XLMR) Workshop in 1995, the genes for Coffin-Lowry, Mohr-Tranebjaerg, and Opitz G/BBB syndromes have been cloned. Jensen syndrome has been found to be allelic to Mohr-Tranebjaerg. Twenty new XLMR syndromes and metabolic or neuromuscular disorders have been reported. Twenty-four new localizations have been established, including five in previously reported conditions (FG, Carpenter, Arts, OPA2, and OFD1). The number of families with… CONTINUE READING
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