Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Journal of Clinical Immunology|April 5, 2024
Proteasome-Associated Syndromes: Updates on Genetics, Clinical Manifestations, Pathogenesis, and TreatmentJiahui Zhang, Panfeng Tao, Natalie T Deuitch, et al.
Genetics in Medicine Open|December 23, 2025
Impact of genomic sequencing information on physicians' treatment recommendations for children with congenital heart diseaseDanton S Char, Natalie T Deuitch, Matthew K Berent, et al.
Blood Advances|June 17, 2026
Functional analysis of germline RUNX1 variants identified in individuals with suspected familial platelet disorderAna Catarina Menezes, Natalie T Deuitch, Aidan Pintuff, et al.
Journal of Genetic Counseling|August 27, 2024
Risk assessment and genetic counseling for hematologic malignancies-Practice resource of the National Society of Genetic CounselorsBrittany L Stewart, Hannah Helber, Sarah A Bannon, et al.
BJC Reports|March 28, 2025
Germline copy number variants in RUNX1: An updated case report and a decade-old red herringNatalie T Deuitch, Amra Kajdic, Erica Bresciani, et al.
Blood Advances|January 30, 2026
Hematologic malignancies in pediatric patients with RUNX1-Familial Platelet Disorder with Associated Myeloid MalignancyAmra Kajdic, Natalie T Deuitch, Erica Bresciani, et al.
Journal of Genetic Counseling|June 7, 2021
"Doctors can read about it, they can know about it, but they've never lived with it": How parents use social media throughout the diagnostic odysseyNatalie T Deuitch, Erika Beckman, Meghan C Halley, et al.
Haematologica|April 2, 2026
Preemptive hematopoietic stem cell transplantation in RUNX1 familial platelet disorder: a shared decision-making frameworkTimothy S Olson, Katrin Ericson, Joseph H Antin, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|December 26, 2025
Deficiency of AP1M2 causes a new autoinflammatory disease with colitisTaijie Jin, Jialin Dai, Chenlu Liu, et al.
Pageof 3