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Rena Zinchenko

Showing results (21-30 of 27) with videos related to

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European Journal of Human Genetics : EJHG|April 13, 2019
Y-chromosomal analysis of clan structure of Kalmyks, the only European Mongol people, and their relationship to Oirat-Mongols of Inner AsiaNatalia Balinova, Helen Post, Alena Kushniarevich, et al.
International Journal of Molecular Sciences|October 16, 2024
A Rare Case of <i>TP63</i>-Associated Lymphopenia Revealed by Newborn Screening Using TRECAndrey Marakhonov, Elena Serebryakova, Anna Mukhina, et al.
Molecular Syndromology|March 2, 2026
Different Diagnoses, Common Ancestry: 22q11.2 Deletion Syndrome and Wiskott-Aldrich Syndrome in the Same FamilyAnastasia Bobreshova, Irina Efimova, Anna Mukhina, et al.
International Journal of Molecular Sciences|April 13, 2023
Clinical and Functional Characteristics of the E92K <i>CFTR</i> Gene Variant in the Russian and Turkish Population of People with Cystic FibrosisElena Kondratyeva, Yuliya Melyanovskaya, Nataliya Bulatenko, et al.
Frontiers in Pediatrics|November 1, 2024
Decreased TREC and KREC levels in newborns with trisomy 21Andrey Marakhonov, Anna Mukhina, Elena Vlasova, et al.
Frontiers in Immunology|February 23, 2026
First 2-year experience of nationwide newborn screening for severe forms of T and B cell immunodeficiency: 2.3 million newborns analyzed using TREC and KREC in RussiaAndrey Marakhonov, Anna Mukhina, Irina Efimova, et al.
Human Mutation|April 14, 2025
The Missing Piece of the Puzzle: Unveiling the Role of <i>PTPN11</i> Gene in Multiple Osteochondromas in a Large Cohort StudyArtem Borovikov, Nailya Galeeva, Andrey Marakhonov, et al.
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Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
European Journal of Human Genetics : EJHG|April 13, 2019
Y-chromosomal analysis of clan structure of Kalmyks, the only European Mongol people, and their relationship to Oirat-Mongols of Inner AsiaNatalia Balinova, Helen Post, Alena Kushniarevich, et al.
International Journal of Molecular Sciences|October 16, 2024
A Rare Case of <i>TP63</i>-Associated Lymphopenia Revealed by Newborn Screening Using TRECAndrey Marakhonov, Elena Serebryakova, Anna Mukhina, et al.
Molecular Syndromology|March 2, 2026
Different Diagnoses, Common Ancestry: 22q11.2 Deletion Syndrome and Wiskott-Aldrich Syndrome in the Same FamilyAnastasia Bobreshova, Irina Efimova, Anna Mukhina, et al.
International Journal of Molecular Sciences|April 13, 2023
Clinical and Functional Characteristics of the E92K <i>CFTR</i> Gene Variant in the Russian and Turkish Population of People with Cystic FibrosisElena Kondratyeva, Yuliya Melyanovskaya, Nataliya Bulatenko, et al.
Frontiers in Pediatrics|November 1, 2024
Decreased TREC and KREC levels in newborns with trisomy 21Andrey Marakhonov, Anna Mukhina, Elena Vlasova, et al.
Frontiers in Immunology|February 23, 2026
First 2-year experience of nationwide newborn screening for severe forms of T and B cell immunodeficiency: 2.3 million newborns analyzed using TREC and KREC in RussiaAndrey Marakhonov, Anna Mukhina, Irina Efimova, et al.
Human Mutation|April 14, 2025
The Missing Piece of the Puzzle: Unveiling the Role of <i>PTPN11</i> Gene in Multiple Osteochondromas in a Large Cohort StudyArtem Borovikov, Nailya Galeeva, Andrey Marakhonov, et al.
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