@article{UBHD-68673301,
  author={Bettendorf, Markus and Fehn, Marita and Grulich-Henn, J{\"u}rgen and Selle, Barbara and Darge, K. and L{\"u}decke, D. K. and Heinrich, Udo and Saeger, W.},
  title={Lymphocytic hypophysitis with central diabetes insipidus and consequent panhypopituitarism preceding a multifocal, intracranial germinoma in a prepubertal girl},
  year={1999},
  pages={288-292},
  language={eng},
  issn={1432-1076},
  volume={158},
  number={4},
  note={Gesehen am 15.12.2020},
  journal={European journal of pediatrics},
  doi={10.1007/s004310051074},
}
@book{UBHD-1219858,
  author={Heinrich, Udo},
  title={Nonsuppressible insulin-like activity (NSILA-S)},
  subtitle={Untersuchungen {\"u}ber die Regulation der NSILA-S-Bildung und die Bedeutung als Wachstumsfaktor unter Verwendung eines neuen, empfindlichen und weitgehend spezifischen kompetitiven Proteinbindungsverfahrens},
  year={1977},
  pages={135 Bl.},
  language={ger},
  school={Heidelberg, Univ., Habil.schr., 1977},
  library={UB [Signatur: 78 Q 975]},
}
@article{UBHD-68718121,
  author={Rao, Ercole and Weiß, Birgit and Fukami, Maki and Mertz, Andrea and Meder, J. and Ogata, Tsutomu and Heinrich, Udo and Garcia-Heras, J. and Schiebel, Katrin and Rappold, Gudrun},
  title={FISH-deletion mapping defines a 270-kb short stature critical interval  in the pseudoautosomal region PAR1 on human sex chromosomes},
  year={1997},
  pages={236-239},
  language={eng},
  issn={1432-1203},
  volume={100},
  number={2},
  note={Gesehen am 30.03.2021},
  journal={Human genetics},
  doi={10.1007/s004390050497},
}
@article{UBHD-68717722,
  author={Rao, Ercole and Weiß, Birgit and Fukami, Maki and Rump, Andreas and Niesler, Beate and Mertz, Annelyse and Muroya, Koji and Binder, Gerhard and Kirsch, Stefan and Winkelmann, Martina and Nordsiek, Gabriele and Heinrich, Udo and Breuning, Martijn H. and Ranke, Michael B. and Rosenthal, André and Ogata, Tsutomu and Rappold, Gudrun},
  title={Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome},
  year={1997},
  pages={54-63},
  language={eng},
  issn={1546-1718},
  volume={16},
  number={1},
  note={Gesehen am 29.03.2021},
  journal={Nature genetics},
  doi={10.1038/ng0597-54},
}
@article{UBHD-68720684,
  author={Rappold, Gudrun and Fukami, Maki and Niesler, Beate and W{\"o}ginger, Simone and Zumkeller, Walter and Bettendorf, Markus and Heinrich, Udo and Vlachopapadoupoulou, Elpis and Reinehr, Thomas and Onigata, Kazumichi and Ogata, Tsutomu},
  title={Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature},
  year={2002},
  pages={1402-1406},
  language={eng},
  issn={1945-7197},
  volume={87},
  number={3},
  note={Gesehen am 07.04.2021},
  journal={The journal of clinical endocrinology & metabolism},
  doi={10.1210/jcem.87.3.8328},
}