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Frontiers in Immunology|January 24, 2020
Sarcoidosis as an Autoimmune DiseaseAnna A Starshinova, Anna M Malkova, Natalia Y Basantsova, et al.
International Journal of Molecular Sciences|October 27, 2022
The Presentation of Two Unrelated Clinical Cases from the Republic of North Ossetia-Alania with the Same Previously Undescribed Variant in the <i>COL6A2</i> GeneSofya A Ionova, Aysylu F Murtazina, Inna S Tebieva, et al.
International Journal of Molecular Sciences|October 16, 2025
13q Deletion Syndrome Presenting with Lymphopenia Detected Through Newborn Screening for Primary ImmunodeficienciesIrina Efimova, Anna Mukhina, Zhanna Markova, et al.
BMC Genomics|April 2, 2022
High frequency of complex CFTR alleles associated with c.1521_1523delCTT (F508del) in Russian cystic fibrosis patientsNika V Petrova, Nataliya Y Kashirskaya, Tatyana A Vasilyeva, et al.
Annals of Human Genetics|January 16, 2015
A clinical and molecular analysis of branchio-oculo-facial syndrome patients in Russia revealed new mutations in TFAP2ATatiana I Meshcheryakova, Rena A Zinchenko, Tatiana A Vasilyeva, et al.
Analytica Chimica Acta|March 19, 2013
Colorimetric test-systems for creatinine detection based on composite molecularly imprinted polymer membranesT A Sergeyeva, L A Gorbach, E V Piletska, et al.
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