Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-Küster-Hauser syndrome.

@article{Ledig2011RecurrentAI,
  title={Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-K{\"u}ster-Hauser syndrome.},
  author={Susanne Ledig and Cordula Schippert and Reiner Strick and Matthias W. Beckmann and Patricia G. Oppelt and Peter F. Wieacker},
  journal={Fertility and sterility},
  year={2011},
  volume={95 5},
  pages={1589-94}
}
OBJECTIVE To identify genetic causes of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. DESIGN Prospective laboratory study. SETTING University hospital. PATIENT(S) Fifty-six patients with MRKH syndrome. INTERVENTION(S) Identification of microdeletions and -duplications in a group of 48 MRKH patients by array-CGH. Results obtained by array-CGH were confirmed by RT-qPCR. Sequential analysis of two candidate genes LHX1 and HNF1B in a group of 56 MRKH patients. MAIN OUTCOME MEASURE(S… CONTINUE READING
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