Searching for genomic variants in IGF2 and CDKN1C in Silver-Russell syndrome patients.

@article{Obermann2004SearchingFG,
  title={Searching for genomic variants in IGF2 and CDKN1C in Silver-Russell syndrome patients.},
  author={Caitriona Obermann and E. F. Meyer and Sebastian Prager and Juergen Tomiuk and Hartmut A. Wollmann and Thomas Eggermann},
  journal={Molecular genetics and metabolism},
  year={2004},
  volume={82 3},
  pages={246-50}
}
Silver-Russell syndrome (SRS) is a heterogeneous syndrome with evidence for a substantial role of genetic factors in its etiology. Apart from other specific clinical features, severe intrauterine and postnatal growth retardation are the dominant characteristics of SRS. Therefore, studies on the genetic basis of the disease focus on genes involved in growth and its regulation. Another key for the identification of (a) SRS gene(s) is the finding of chromosomal disturbances in SRS patients… CONTINUE READING
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