R V Magzhanov - JoVE Visualize

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

Pageof 3

Sort By:

You have reached the last page of results.This site can display upto 30 results.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|June 16, 2017

[L-2-hydroxyglutaric aciduria caused by a new mutation in the L2HGDH gene]E V Saifullina, E Yu Zakharova, M V Kurkina, et al.

Genetika|November 30, 2000

[Expansion and mutation rate in CTG repeats in the myotonic dystrophy gene]I M Khidiiatova, R I Fatkhlislamova, R V Magzhanov, et al.

Genetika|July 31, 2008

[Analysis of the association of allelic variants of apolypoprotein E and interleukin 1 beta genes with multiple sclerosis in ethnic Tatars]O E Mustafina, K Z Bakhtiiarova, A M Mikhaĭlova, et al.

Genetika|June 19, 2009

[Polymorphism of the prion protein PRNP gene and risk of multiple sclerosis development in ethnic Russians from Bashkortostan]O V Chubukova, O E Mustafina, A V Chemeris, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|April 18, 2002

[CTG-repeat analysis of myotonin protein kinase gene in Bashkortostan patients with myotonic dystrophy]I M Khidiiatova, R I Fatkhlislamova, R V magzhanov, et al.

Genetika|August 3, 2000

[Analysis of expansion of the triplet repeat (CTG)n in myotonic dystrophy patients from Bashkir]P A Slominskiĭ, S N Popova, R I Fatkhlislamova, et al.

Genetika|January 24, 2014

[MFN2 gene analysis in patients with hereditary motor and sensory neuropathy from Bashkortostan Republic]I M Khidiyatova, I A Skachkova, E V Saifullina, et al.

Genetika|April 3, 2003

[Analysis of deletion mutations in the PARK2 gene in idiopathic Parkinson's disease]P A Slominskiĭ, O V Miloserdova, S N Popova, et al.

Genetika|December 10, 2008

[Spectrum and frequency of mutations in the connexin 32 gene (GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan]I M Khidiianova, E G Bagautdinova, D V Galieva, et al.

Molekuliarnaia Biologiia|January 15, 2009

[Polymorphism of APOE gene and risk of development of the multiple sclerosis at ethnic Russians]O E Mustafina, A M Mikhaĭlova, K Z Bakhtiiarova, et al.

Pageof 3

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

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 30 results.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|June 16, 2017

[L-2-hydroxyglutaric aciduria caused by a new mutation in the L2HGDH gene]E V Saifullina, E Yu Zakharova, M V Kurkina, et al.

Genetika|November 30, 2000

[Expansion and mutation rate in CTG repeats in the myotonic dystrophy gene]I M Khidiiatova, R I Fatkhlislamova, R V Magzhanov, et al.

Genetika|July 31, 2008

[Analysis of the association of allelic variants of apolypoprotein E and interleukin 1 beta genes with multiple sclerosis in ethnic Tatars]O E Mustafina, K Z Bakhtiiarova, A M Mikhaĭlova, et al.

Genetika|June 19, 2009

[Polymorphism of the prion protein PRNP gene and risk of multiple sclerosis development in ethnic Russians from Bashkortostan]O V Chubukova, O E Mustafina, A V Chemeris, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|April 18, 2002

[CTG-repeat analysis of myotonin protein kinase gene in Bashkortostan patients with myotonic dystrophy]I M Khidiiatova, R I Fatkhlislamova, R V magzhanov, et al.

Genetika|August 3, 2000

[Analysis of expansion of the triplet repeat (CTG)n in myotonic dystrophy patients from Bashkir]P A Slominskiĭ, S N Popova, R I Fatkhlislamova, et al.

Genetika|January 24, 2014

[MFN2 gene analysis in patients with hereditary motor and sensory neuropathy from Bashkortostan Republic]I M Khidiyatova, I A Skachkova, E V Saifullina, et al.

Genetika|April 3, 2003

[Analysis of deletion mutations in the PARK2 gene in idiopathic Parkinson's disease]P A Slominskiĭ, O V Miloserdova, S N Popova, et al.

Genetika|December 10, 2008

[Spectrum and frequency of mutations in the connexin 32 gene (GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan]I M Khidiianova, E G Bagautdinova, D V Galieva, et al.

Molekuliarnaia Biologiia|January 15, 2009

[Polymorphism of APOE gene and risk of development of the multiple sclerosis at ethnic Russians]O E Mustafina, A M Mikhaĭlova, K Z Bakhtiiarova, et al.

Pageof 3