Your browser doesn't support javascript.
loading
[Molecular genetics in diagnosis of Coats disease: combination of oligogenic variants associated with different forms of hereditary retinal dystrophy]. / Molekulyarno-geneticheskie nakhodki pri diagnostike bolezni Koatsa: sochetanie oligolokusnykh izmenenii, svyazannykh s raznymi nozologicheskimi formami nasledstvennoi retinopatii.
Vasilyeva, T A; Kadyshev, V V; Marakhonov, A V; Kanivets, I V; Korostelev, S A; Koshkin, P A; Pyankov, D V; Petrova, N V; Kutsev, S I; Zinchenko, R A.
Afiliação
  • Vasilyeva TA; Research Centre for Medical Genetics, Moscow, Russia.
  • Kadyshev VV; Research Centre for Medical Genetics, Moscow, Russia.
  • Marakhonov AV; Research Centre for Medical Genetics, Moscow, Russia.
  • Kanivets IV; Russian Medical Academy of Continuous Professional Education, Moscow, Russia.
  • Korostelev SA; OOO Genomed, Moscow, Russia.
  • Koshkin PA; OOO Genomed, Moscow, Russia.
  • Pyankov DV; I.M. Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia.
  • Petrova NV; OOO Genomed, Moscow, Russia.
  • Kutsev SI; OOO Genomed, Moscow, Russia.
  • Zinchenko RA; Research Centre for Medical Genetics, Moscow, Russia.
Vestn Oftalmol ; 139(1): 69-74, 2023.
Article em Ru | MEDLINE | ID: mdl-36924516
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Retinose Pigmentar / Distrofias Retinianas / Telangiectasia Retiniana Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: Ru Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Retinose Pigmentar / Distrofias Retinianas / Telangiectasia Retiniana Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: Ru Ano de publicação: 2023 Tipo de documento: Article