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Author/Creator Merki, Yvonne

1. Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles. (8th March 2017)

Authors:
Gourri, Elise; Denomme, Gregory A.; Merki, Yvonne; Scharberg, Erwin A.; Vrignaud, Cedric; Frey, Beat M.; Peyrard, Thierry; Gassner, Christoph
Journal:
British journal of haematology
Issue:
Volume 177:Number 4(2017)
Page Start:
630
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Stepwise partitioning of Xp21: a profiling method for XK deletions causative of the McLeod syndrome. Issue 9 (28th May 2017)

Authors:
Gassner, Christoph; Brönnimann, Chantal; Merki, Yvonne; Mattle‐Greminger, Maja P.; Sigurdardottir, Sonja; Meyer, Eduardo; Engström, Charlotte; O'Sullivan, John D.; Jung, Hans H.; Frey, Beat M.
Journal:
Transfusion
Issue:
Volume 57:Issue 9(2017)
Page Start:
2125
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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