@book{UBHD-68716753,
  author={Buselmaier, Werner and Tariverdian, Gholamali},
  title={Humangenetik},
  edition={Zweite, v{\"o}llig neu bearbeitete Auflage},
  publisher={Springer Berlin Heidelberg},
  address={Berlin, Heidelberg ; s.l.},
  year={1999},
  pages={Online-Ressource (XIV, 450 S.)},
  language={ger},
  isbn={978-3-662-07818-1},
  series={Springer-Lehrbuch},
  note={Gesehen am 25.03.2021},
  doi={10.1007/978-3-662-07818-1},
}
@book{UBHD-19982208,
  author={Buselmaier, Werner and Tariverdian, Gholamali},
  title={Humangenetik},
  edition={2., v{\"o}llig neu bearb. Aufl.},
  publisher={Springer},
  address={Berlin ; Heidelberg [u.a.]},
  year={1999},
  pages={XIV, 449 S.},
  language={ger},
  isbn={978-3-540-63430-0 and 3-540-63430-4},
  series={Springer-Lehrbuch},
  keywords={Humangenetik ; Humangenetik},
  library={MG [Signatur: Co 498]},
}
@article{UBHD-69205703,
  author={Drechsler, Matthias and Meijers-Heijboer, E. J. and Schneider, S. and Schurich, B{\"a}rbel and Grond-Ginsbach, Caspar and Tariverdian, Gholamali and Kantner, G. and Blankenagel, Anita and Kaps, D. and Schroeder-Kurth, Traute and Royer-Pokora, Brigitte},
  title={Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene},
  year={1994},
  pages={331-338},
  language={eng},
  issn={1432-1203},
  volume={94},
  number={4},
  note={Gesehen am 18.04.2024},
  journal={Human genetics},
  doi={10.1007/BF00201588},
}
@article{UBHD-68670395,
  author={Schilke, Kathrin and Schaefer, Franz and Waldherr, R{\"u}diger and Rohrschneider, Wiltrud and John, Christoph and Himbert, Urban and Mayatepek, Ertan and Tariverdian, Gholamali},
  title={A case of Perlman syndrome},
  subtitle={fetal gigantism, renal dysplasia, and severe neurological deficits},
  year={2000},
  pages={29-33},
  language={eng},
  issn={1096-8628},
  volume={91},
  number={1},
  note={Gesehen am 08.12.2020},
  journal={American journal of medical genetics},
  doi={10.1002/(SICI)1096-8628(20000306)91:1<29::AID-AJMG5>3.0.CO;2-U},
}
@article{UBHD-68688053,
  author={Schulze, Birgit R. and Horn, Denise and Kobelt, Albrecht and Tariverdian, Gholamali and Stellzig-Eisenhauer, Angelika},
  title={Rare dental abnormalities seen in oculo-facio-cardio-dental (OFCD) syndrome},
  subtitle={three new cases and review of nine patients},
  year={1999},
  pages={429-435},
  language={eng},
  issn={1096-8628},
  volume={82},
  number={5},
  note={Gesehen am 03.02.2021},
  journal={American journal of medical genetics},
  doi={10.1002/(SICI)1096-8628(19990219)82:5<429::AID-AJMG13>3.0.CO;2-S},
}
@article{UBHD-68669417,
  author={Spranger, Stephanie and W{\"o}ginger, Simone and Jauch, Anna and Wolff, Kathrin and Rauterberg-Ruland, Inge and Hager, Dieter and Tariverdian, Gholamali and Tr{\"o}ger, Jochen and Rappold, Gudrun},
  title={Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3},
  year={1999},
  pages={367-371},
  language={eng},
  issn={1096-8628},
  volume={83},
  number={5},
  note={Gesehen am 04.12.2020},
  journal={American journal of medical genetics},
  doi={10.1002/(SICI)1096-8628(19990423)83:5<367::AID-AJMG5>3.0.CO;2-K},
}
@article{UBHD-69114569,
  author={Spranger, Stephanie and Tariverdian, Gholamali and Albert, Friedrich and Sontheimer, Dieter and Z{\"o}ller, Joachim E. and Weber, M. and Tr{\"o}ger, Jochen},
  title={Microcephalic osteodysplastic primordial dwarfism type II},
  subtitle={a child with unusual symptoms and clinical course; a case report},
  year={1996},
  pages={796-799},
  language={eng},
  issn={1432-1076},
  volume={155},
  number={9},
  note={Gesehen am 21.08.2023},
  journal={European journal of pediatrics},
  doi={10.1007/BF02002910},
}
@article{UBHD-69205802,
  author={Spranger, Stephanie and Stute, Heiko and Blankenagel, Anita and Jauch, Anna and Hager-Czuday, Doris and Tariverdian, Gholamali},
  title={MIDAS-Syndrom},
  subtitle={eine X-chromosomale Erkrankung; Differentialdiagnose zum kongenitalen Varizellensyndrom},
  year={1998},
  pages={761-765},
  language={ger},
  issn={1433-0474},
  volume={146},
  number={8},
  note={Gesehen am 18.04.2024},
  journal={Monatsschrift Kinderheilkunde},
  doi={10.1007/s001120050319},
}
@book{UBHD-9910609,
  author={Tariverdian, Gholamali and Paul, Marion},
  editor={Paul, Marion},
  title={Genetische Diagnostik in Geburtshilfe und Gyn{\"a}kologie},
  subtitle={Leitfaden f{\"u}r Klinik und Praxis : mit 256 Abbildungen},
  publisher={Springer},
  address={Berlin ; Heidelberg ; New York ; Barcelona},
  year={1999},
  pages={XVI, 538 Seiten},
  language={ger},
  isbn={3-540-65328-7 and 978-3-540-65328-8},
  note={Literaturangaben},
  keywords={Pr{\"a}natale Diagnostik / Ultraschalldiagnostik ; Genetische Beratung ; Erbkrankheit ; Geburtshilfe / Gyn{\"a}kologie},
  library={UB [Signatur: UBN/YQ 2514 T186] ; MG [Signatur: Co 497] ; UW [Signatur: J 1 c]},
}