Search

Author/Creator Seidel, Markus G

1. A novel immunodeficiency syndrome associated with partial trisomy 19p13. Issue 4 (15th January 2014)

Authors:
Seidel, Markus G; Duerr, Celia; Woutsas, Stavroula; Schwerin-Nagel, Anette; Sadeghi, Kambis; Neesen, Jürgen; Uhrig, Sabine; Santos-Valente, Elisangela; Pickl, Winfried F; Schwinger, Wolfgang; Urban, Christian; Boztug, Kaan; Förster-Waldl, Elisabeth
Journal:
Journal of medical genetics
Issue:
Volume 51:Issue 4(2014)
Page Start:
254
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Novel phenotypes observed in patients with ETV6-linked leukaemia/familial thrombocytopenia syndrome and a biallelic ARID5B risk allele as leukaemogenic cofactor. Issue 6 (8th November 2019)

Authors:
Karastaneva, Anna; Nebral, Karin; Schlagenhauf, Axel; Baschin, Marcel; Palankar, Raghavendra; Juch, Herbert; Heitzer, Ellen; Speicher, Michael R; Höfler, Gerald; Grigorow, Irina; Urban, Christian; Benesch, Martin; Greinacher, Andreas; Haas, Oskar A; Seidel, Markus G
Journal:
Journal of medical genetics
Issue:
Volume 57:Issue 6(2020)
Page Start:
427
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. The Human Phenotype Ontology in 2021. Issue Volume 49:Issue D1(2021) (2nd December 2020)

Authors:
Köhler, Sebastian; Gargano, Michael; Matentzoglu, Nicolas; Carmody, Leigh C; Lewis-Smith, David; Vasilevsky, Nicole A; Danis, Daniel; Balagura, Ganna; Baynam, Gareth; Brower, Amy M; Callahan, Tiffany J; Chute, Christopher G; Est, Johanna L; Galer, Peter D; Ganesan, Shiva; Griese, Matthias; Haimel...
Journal:
Nucleic acids research
Issue:
Volume 49:Issue D1(2021)
Page Start:
D1207
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗