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The Journal of Allergy and Clinical Immunology
|
May 25, 2021
Rubella vaccine-induced granulomas are a novel phenotype with incomplete penetrance of genetic defects in cytotoxicity
Miriam Groß, Carsten Speckmann, Annette May, et al.
Nature Communications
|
October 4, 2019
Publisher Correction: Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis
Nina K Serwas, Birgit Hoeger, Rico C Ardy, et al.
Nature Communications
|
July 17, 2019
Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis
Nina K Serwas, Birgit Hoeger, Rico C Ardy, et al.
The Lancet Regional Health. Europe
|
May 28, 2024
Diagnostic yield and clinical impact of germline sequencing in children with CNS and extracranial solid tumors-a nationwide, prospective Swedish study
Bianca Tesi, Kristina Lagerstedt Robinson, Frida Abel, et al.
Genome Medicine
|
March 17, 2021
Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients
Henrik Stranneheim, Kristina Lagerstedt-Robinson, Måns Magnusson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 28, 2025
The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)
Linda A J Hendricks, Katja C J Verbeek, Janneke H M Schuurs-Hoeijmakers, et al.
Genome Medicine
|
March 31, 2026
The genomic medicine center Karolinska 10-year report on genome sequencing for rare diseases and a strategy for stepwise clinical implementation
Anna Lindstrand, Kristina Lagerstedt-Robinson, Anders Jemt, et al.
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Search research articles
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Showing results (61-70 of 67) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 67 results.
The Journal of Allergy and Clinical Immunology
|
May 25, 2021
Rubella vaccine-induced granulomas are a novel phenotype with incomplete penetrance of genetic defects in cytotoxicity
Miriam Groß, Carsten Speckmann, Annette May, et al.
Nature Communications
|
October 4, 2019
Publisher Correction: Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis
Nina K Serwas, Birgit Hoeger, Rico C Ardy, et al.
Nature Communications
|
July 17, 2019
Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis
Nina K Serwas, Birgit Hoeger, Rico C Ardy, et al.
The Lancet Regional Health. Europe
|
May 28, 2024
Diagnostic yield and clinical impact of germline sequencing in children with CNS and extracranial solid tumors-a nationwide, prospective Swedish study
Bianca Tesi, Kristina Lagerstedt Robinson, Frida Abel, et al.
Genome Medicine
|
March 17, 2021
Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients
Henrik Stranneheim, Kristina Lagerstedt-Robinson, Måns Magnusson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 28, 2025
The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)
Linda A J Hendricks, Katja C J Verbeek, Janneke H M Schuurs-Hoeijmakers, et al.
Genome Medicine
|
March 31, 2026
The genomic medicine center Karolinska 10-year report on genome sequencing for rare diseases and a strategy for stepwise clinical implementation
Anna Lindstrand, Kristina Lagerstedt-Robinson, Anders Jemt, et al.
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of 7