Turner syndrome and Xp deletions: clinical and molecular studies in 47 patients.

@article{Ogata2001TurnerSA,
  title={Turner syndrome and Xp deletions: clinical and molecular studies in 47 patients.},
  author={Tsutomu Ogata and Koji Muroya and Nobutake Matsuo and Osamu Shinohara and Tohru Yorifuji and Yoshikazu Nishi and Yukihiro Hasegawa and Reiko Horikawa and Katsuhiko Tachibana},
  journal={The Journal of clinical endocrinology and metabolism},
  year={2001},
  volume={86 11},
  pages={
          5498-508
        }
}
Although clinical features of Turner syndrome have primarily been explained by the dosage effects of SHOX (short stature homeobox-containing gene) and the putative lymphogenic gene together with chromosomal effects leading to nonspecific features, several matters remain to be determined, including modifying factors for the effects of SHOX haploinsufficiency, chromosomal location of the lymphogenic gene, and genetic factors for miscellaneous features such as multiple pigmented nevi. To clarify… CONTINUE READING

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