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

  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},
  volume={95 5},
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
37 Citations
23 References
Similar Papers


Publications citing this paper.
Showing 1-10 of 37 extracted citations


Publications referenced by this paper.
Showing 1-10 of 23 references

Two cases of Mayer-Rokitansky-Kuster-Hauser syndrome with situs inversus totalis: coincidence or co-existence

  • H Ozkurt, MM Cenker, F Ksekiner, M. Basak
  • J Pediatr Adolesc Gynecol 2009;22:
  • 2009

Programme de recherches sur les aplasies M€ull eriennes. Guerrier D. MayerRokitansky-K€uster-Hauser (MRKH) syndrome

  • K Morcel, L. Camborieux
  • Orphanet J Rare Dis 2007;2:13
  • 2007

Similar Papers

Loading similar papers…