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Richard Maas

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Molecular Genetics & Genomic Medicine|October 6, 2015
Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative diseaseSameer S Chopra, Ignaty Leshchiner, Hatice Duzkale, et al.
Blood|December 14, 2023
Low-frequency inherited complement receptor variants are associated with purpura fulminansPavan K Bendapudi, Sumaiya Nazeen, Justine Ryu, et al.
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Showing results (11-20 of 12) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 12 results.
Molecular Genetics & Genomic Medicine|October 6, 2015
Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative diseaseSameer S Chopra, Ignaty Leshchiner, Hatice Duzkale, et al.
Blood|December 14, 2023
Low-frequency inherited complement receptor variants are associated with purpura fulminansPavan K Bendapudi, Sumaiya Nazeen, Justine Ryu, et al.
Pageof 2