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BMC Genomics
|
April 2, 2022
High frequency of complex CFTR alleles associated with c.1521_1523delCTT (F508del) in Russian cystic fibrosis patients
Nika 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 TFAP2A
Tatiana I Meshcheryakova, Rena A Zinchenko, Tatiana A Vasilyeva, et al.
Genetika
|
June 19, 2009
[Genetic epidemiological study of Bashkortostan Republic: the diversity of monogenic hereditary diseases in five districts]
R A Zinchenko, S Sh Murzabaeva, Ia I Grinberg, et al.
Analytica Chimica Acta
|
March 19, 2013
Colorimetric test-systems for creatinine detection based on composite molecularly imprinted polymer membranes
T A Sergeyeva, L A Gorbach, E V Piletska, et al.
Vestnik Oftalmologii
|
March 16, 2023
[Molecular genetics in diagnosis of Coats disease: combination of oligogenic variants associated with different forms of hereditary retinal dystrophy]
T A Vasilyeva, V V Kadyshev, A V Marakhonov, et al.
Genetika
|
June 11, 2009
[Epidemiology of monogenic hereditary diseases in Rostov oblast: population dynamic factors determining the differentiation of the load of hereditary diseases in eight districts]
R A Zinchenko, S S Amelina, R A Shokarev, et al.
International Journal of Molecular Sciences
|
March 11, 2023
Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report
Tatyana A Vasilyeva, Andrey V Marakhonov, Inna S Tebieva, et al.
Genetika
|
April 2, 2009
[Epidemiology of monogenic hereditary diseases in Rostov Oblast: population dynamic factors determining the differentiation of the load of hereditary diseases in eight districts]
R A Zinchenko, S S Amelina, G I El'chinova, et al.
BMC Medical Genetics
|
October 23, 2020
Prenatal diagnosis of Norrie disease after whole exome sequencing of an affected proband during an ongoing pregnancy: a case report
Andrey V Marakhonov, Irina A Mishina, Vitaly V Kadyshev, et al.
Journal of Aging Research
|
September 22, 2025
Variation in the Content of Three Tandem Repeats of the Human Genome (Ribosomal, Satellite III, and Telomere) in Peripheral Blood Leukocyte DNA of People of Different Ages (5-101 Years)
E S Ershova, P E Umriukhin, R A Zinchenko, et al.
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Search research articles
Search
Showing results (151-160 of 192) with videos related to
Sort By:
Page
of 20
BMC Genomics
|
April 2, 2022
High frequency of complex CFTR alleles associated with c.1521_1523delCTT (F508del) in Russian cystic fibrosis patients
Nika 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 TFAP2A
Tatiana I Meshcheryakova, Rena A Zinchenko, Tatiana A Vasilyeva, et al.
Genetika
|
June 19, 2009
[Genetic epidemiological study of Bashkortostan Republic: the diversity of monogenic hereditary diseases in five districts]
R A Zinchenko, S Sh Murzabaeva, Ia I Grinberg, et al.
Analytica Chimica Acta
|
March 19, 2013
Colorimetric test-systems for creatinine detection based on composite molecularly imprinted polymer membranes
T A Sergeyeva, L A Gorbach, E V Piletska, et al.
Vestnik Oftalmologii
|
March 16, 2023
[Molecular genetics in diagnosis of Coats disease: combination of oligogenic variants associated with different forms of hereditary retinal dystrophy]
T A Vasilyeva, V V Kadyshev, A V Marakhonov, et al.
Genetika
|
June 11, 2009
[Epidemiology of monogenic hereditary diseases in Rostov oblast: population dynamic factors determining the differentiation of the load of hereditary diseases in eight districts]
R A Zinchenko, S S Amelina, R A Shokarev, et al.
International Journal of Molecular Sciences
|
March 11, 2023
Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report
Tatyana A Vasilyeva, Andrey V Marakhonov, Inna S Tebieva, et al.
Genetika
|
April 2, 2009
[Epidemiology of monogenic hereditary diseases in Rostov Oblast: population dynamic factors determining the differentiation of the load of hereditary diseases in eight districts]
R A Zinchenko, S S Amelina, G I El'chinova, et al.
BMC Medical Genetics
|
October 23, 2020
Prenatal diagnosis of Norrie disease after whole exome sequencing of an affected proband during an ongoing pregnancy: a case report
Andrey V Marakhonov, Irina A Mishina, Vitaly V Kadyshev, et al.
Journal of Aging Research
|
September 22, 2025
Variation in the Content of Three Tandem Repeats of the Human Genome (Ribosomal, Satellite III, and Telomere) in Peripheral Blood Leukocyte DNA of People of Different Ages (5-101 Years)
E S Ershova, P E Umriukhin, R A Zinchenko, et al.
Page
of 20