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A Zinchenko

Showing results (141-150 of 192) with videos related to

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Genetika|February 26, 2015
[The load and diversity of hereditary diseases in four raions of Rostov oblast]S S Amelina, N V Vetrova, M A Amelina, et al.
European Journal of Human Genetics : EJHG|January 29, 2009
Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effectElena A Bliznetz, Svetlana M Tverskaya, Rena A Zinchenko, et al.
Current Issues in Molecular Biology|January 22, 2024
An Unusual Presentation of Novel Missense Variant in <i>PAX6</i> Gene: NM_000280.4:c.341A>G, p.(Asn114Ser)Tatyana A Vasilyeva, Natella V Sukhanova, Olga V Khalanskaya, et al.
Vestnik Oftalmologii|October 26, 2022
[Gyrate atrophy of the choroid and retina with ornithinemia and foveoschisis (clinical observation)]I V Zolnikova, S V Milash, R A Zinchenko, et al.
Frontiers in Genetics|September 16, 2021
Epidemiology of Rare Hereditary Diseases in the European Part of Russia: Point and Cumulative PrevalenceRena A Zinchenko, Eugeny K Ginter, Andrey V Marakhonov, et al.
Frontiers in Genetics|September 26, 2022
Corrigendum: Epidemiology of rare hereditary diseases in the European part of Russia: Point and cumulative prevalenceRena A Zinchenko, Eugeny K Ginter, Andrey V Marakhonov, et al.
Journal of Medical Genetics|May 30, 2020
Analysis of genotype-phenotype correlations in <i>PAX6</i>-associated aniridiaTatyana A Vasilyeva, Andrey V Marakhonov, Anna A Voskresenskaya, et al.
BMC Medical Genomics|March 6, 2018
Primary microcephaly case from the Karachay-Cherkess Republic poses an additional support for microcephaly and Seckel syndrome spectrum disordersAndrey V Marakhonov, Fedor A Konovalov, Amin Kh Makaov, et al.
Biochemistry. Biokhimiia|November 17, 2015
Truncated Variants of Serratia proteamaculans Oligopeptidase B Having Different ActivitiesA G Mikhailova, A N Nekrasov, A A Zinchenko, 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.
Pageof 20

Showing results (141-150 of 192) with videos related to

Sort By:
Pageof 20
Genetika|February 26, 2015
[The load and diversity of hereditary diseases in four raions of Rostov oblast]S S Amelina, N V Vetrova, M A Amelina, et al.
European Journal of Human Genetics : EJHG|January 29, 2009
Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effectElena A Bliznetz, Svetlana M Tverskaya, Rena A Zinchenko, et al.
Current Issues in Molecular Biology|January 22, 2024
An Unusual Presentation of Novel Missense Variant in <i>PAX6</i> Gene: NM_000280.4:c.341A>G, p.(Asn114Ser)Tatyana A Vasilyeva, Natella V Sukhanova, Olga V Khalanskaya, et al.
Vestnik Oftalmologii|October 26, 2022
[Gyrate atrophy of the choroid and retina with ornithinemia and foveoschisis (clinical observation)]I V Zolnikova, S V Milash, R A Zinchenko, et al.
Frontiers in Genetics|September 16, 2021
Epidemiology of Rare Hereditary Diseases in the European Part of Russia: Point and Cumulative PrevalenceRena A Zinchenko, Eugeny K Ginter, Andrey V Marakhonov, et al.
Frontiers in Genetics|September 26, 2022
Corrigendum: Epidemiology of rare hereditary diseases in the European part of Russia: Point and cumulative prevalenceRena A Zinchenko, Eugeny K Ginter, Andrey V Marakhonov, et al.
Journal of Medical Genetics|May 30, 2020
Analysis of genotype-phenotype correlations in <i>PAX6</i>-associated aniridiaTatyana A Vasilyeva, Andrey V Marakhonov, Anna A Voskresenskaya, et al.
BMC Medical Genomics|March 6, 2018
Primary microcephaly case from the Karachay-Cherkess Republic poses an additional support for microcephaly and Seckel syndrome spectrum disordersAndrey V Marakhonov, Fedor A Konovalov, Amin Kh Makaov, et al.
Biochemistry. Biokhimiia|November 17, 2015
Truncated Variants of Serratia proteamaculans Oligopeptidase B Having Different ActivitiesA G Mikhailova, A N Nekrasov, A A Zinchenko, 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.
Pageof 20