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Author/Creator Sorge, Ina

2. Genotype–phenotype correlation at codon 1740 of SETD2. Issue 9 (24th July 2020)

Authors:
Rabin, Rachel; Radmanesh, Alireza; Glass, Ian A.; Dobyns, William B.; Aldinger, Kimberly A.; Shieh, Joseph T.; Romoser, Shelby; Bombei, Hannah; Dowsett, Leah; Trapane, Pamela; Bernat, John A.; Baker, Janice; Mendelsohn, Nancy J.; Popp, Bernt; Siekmeyer, Manuela; Sorge, Ina; Sansbury, Francis Hugh...
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 9(2020)
Page Start:
2037
Record Type:
Journal Article
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5. The constitutional gain‐of‐function variant p.Glu1099Lys in NSD2 is associated with a novel syndrome. Issue 2 (20th October 2022)

Authors:
Popp, Bernt; Brugger, Melanie; Poschmann, Sibylle; Bartolomaeus, Tobias; Radtke, Maximilian; Hentschel, Julia; Di Donato, Nataliya; Rump, Andreas; Gburek‐Augustat, Janina; Graf, Elisabeth; Wagner, Matias; Sorge, Ina; Lemke, Johannes R; Meitinger, Thomas; Abou Jamra, Rami; Strehlow, Vincent; Brune...
Journal:
Clinical genetics
Issue:
Volume 103:Issue 2(2023)
Page Start:
226
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗