['Synthetic' maps of the Mari gene pool (from immunobiochemical polymorphism data)]

Autor: Op, Balanovskiĭ, Sd, Nurbaev, Oi, Kravchuk, Sv, Makarov, Viktor Spitsyn, Ek, Ginter

Publikováno v: Europe PubMed Central

Models of geographic distribution of 33 alleles of 10 loci (AB0, TF, GC, PI, HP, AHS, F13B, ACP1, PGM1, GLO1) in the indigenous population of five raions (districts) of Marii El Republic were analyzed by cartographic statistical methods. Based on 33

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::56715eee6e57cbc71310a3a3c8566bab
https://pubmed.ncbi.nlm.nih.gov/10330615

Inherited thrombophilia: Part 2

Autor: Da, Lane, Pm, Mannucci, Ka, Bauer, Rm, Bertina, Np, Bochkov, Boulyjenkov V, Chandy M, Bjorn Dahlback, Ek, Ginter, Jp, Miletich, Fr, Rosendaal, Seligsohn U

Publikováno v: Europe PubMed Central

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::138fbd084cd70209e723cc89f9d88846
https://pubmed.ncbi.nlm.nih.gov/8971998

[Further analysis of location of the gene for inborn dominant Nochurli cataract]

Autor: Ek, Ginter, Ei, Rogaev, Gi, Korovaĭtseva, Turaeva ShM, An, Petrin, Viktor Spitsyn, Lv, Tarlycheva

Publikováno v: Europe PubMed Central

The study of location of the gene for inborn dominant nokhur kataracta is going on. No linkage of this gene with the locus of alpha-globin gene (16p13.3) and the locus (7q36-qter) was revealed. Additional evidence was obtained for a possible location

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4a37459cd32387f8a75e3171a923f1ce
https://pubmed.ncbi.nlm.nih.gov/8354473

[An attempt to locate the gene for congenital cataracts using linkage analysis]

Autor: Ek, Ginter, An, Petrin, Viktor Spitsyn, Ei, Rogaev

Publikováno v: Europe PubMed Central

Analysis of linkage between the gene of autosomal dominant congenital cataract and 10 polymorphic loci localized in 1, 2, 3, 4, 6, 13, 16 chromosomes was performed. Some loci were only informative for this purpose: Mucin located in 1q21, NH24 located

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1a58f760d8c8a0f5b0455f1d8475665f
http://europepmc.org/abstract/med/1778455

The Study of the Inheritance Mechanisms of Myotonic Dystrophy Type 1 (DM1) in Families from the Republic of North Ossetia-Alania.

Autor: Ionova SA; Research Centre for Medical Genetics, Moskvorechie Str. 1, 115522 Moscow, Russia., Murtazina AF; Research Centre for Medical Genetics, Moskvorechie Str. 1, 115522 Moscow, Russia., Marakhonov AA; Research Centre for Medical Genetics, Moskvorechie Str. 1, 115522 Moscow, Russia., Shchagina OA; Research Centre for Medical Genetics, Moskvorechie Str. 1, 115522 Moscow, Russia., Ryadninskaya NV; Research Centre for Medical Genetics, Moskvorechie Str. 1, 115522 Moscow, Russia., Tebieva IS; North Ossetian State Medical Academy of the Ministry of Health of the Russian Federation, Pushkinskaya St., 40, Republic of North Ossetia-Alania, 362019 Vladikavkaz, Russia.; Medical and Genetic Consultation of the Republican Children's Clinical Hospital of the Republic of North Ossetia-Alania, Barbashova 33A, 362020 Vladikavkaz, Russia., Kadyshev VV; Research Centre for Medical Genetics, Moskvorechie Str. 1, 115522 Moscow, Russia., Borovikov AO; Research Centre for Medical Genetics, Moskvorechie Str. 1, 115522 Moscow, Russia., Ginter EK; Research Centre for Medical Genetics, Moskvorechie Str. 1, 115522 Moscow, Russia., Kutsev SI; Research Centre for Medical Genetics, Moskvorechie Str. 1, 115522 Moscow, Russia., Zinchenko RA; Research Centre for Medical Genetics, Moskvorechie Str. 1, 115522 Moscow, Russia.

Publikováno v: International journal of molecular sciences [Int J Mol Sci] 2024 Sep 09; Vol. 25 (17). Date of Electronic Publication: 2024 Sep 09.