Browsing Universitätsbibliographie by Author "Singer, Sylke"

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12q24.33 Deletion: Report of a Patient With Intellectual Disability and Review of the Literature

Kehrer, Martin; Singer, Sylke; Grasshoff, Ute; Schaeferhoff, Karin; Bonin, Michael; Riess, Olaf; Schoening, Martin; Tzschach, Andreas (2013)
Discordance between ultrasound and cell free DNA screening for monosomy X

Kagan, Karl Oliver; Hoopmann, Markus; Singer, Sylke; Schaeferhoff, Karin; Dufke, Andreas; Mau-Holzmann, Ulrike A. (2016)
Interstitial Duplication of Chromosome Region 1q25.1q25.3: Report of a Patient With Mild Cognitive Deficits, Tall Stature and Facial Dysmorphisms

Kehrer, Martin; Liehr, Thomas; Benkert, Tanja; Singer, Sylke; Grasshoff, Ute; Schaeferhoff, Karin; Bonin, Michael; Weichselbaum, Annette; Tzschach, Andreas (2015)
Parental Origin of de novo Cytogenetically Balanced Reciprocal Non-Robertsonian Translocations

Hoeckner, M.; Spreiz, A.; Fruehmesser, A.; Tzschach, A.; Dufke, A.; Rittinger, O.; Kalscheuer, V.; Singer, S.; Erdel, M.; Fauth, C.; Grossmann, V.; Utermann, G.; Zschocke, J.; Kotzot, D. (2012)
Parental origin of deletions and duplications - about the necessity to check for cryptic inversions

Liehr, Thomas; Schreyer, Isolde; Kuechler, Alma; Manolakos, Emmanouil; Singer, Sylke; Dufke, Andreas; Wilhelm, Kathleen; Jancuskova, Tereza; Cmejla, Radek; Othman, Moneeb A. K.; Al-Rikabi, Ahmed H.; Mrasek, Kristin; Ziegler, Monika; Kankel, Stefanie; Kreskowski, Katharina; Weise, Anja (2018)
Pre- and postnatal findings in a patient with a recombinant chromosome rec(8)(qter -> q21.11::p23.3 -> qter) due to a paternal pericentric inversion inv(8)(p23.3q21.11) and review of the literature

Habhab, Wisam; Mau-Holzmann, Ulrike; Singer, Sylke; Rie, Angelika; Kagan, Karl-Oliver; Gerbig, Ines; Schaeferhoff, Karin; Dufke, Andreas; Kehrer, Martin (2020)

Now showing items 1-6 of 6

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