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Primary microcephaly case from the Karachay-Cherkess Republic poses an additional support for microcephaly and Seckel syndrome spectrum disorders.
Marakhonov, Andrey V; Konovalov, Fedor A; Makaov, Amin Kh; Vasilyeva, Tatyana A; Kadyshev, Vitaly V; Galkina, Varvara A; Dadali, Elena L; Kutsev, Sergey I; Zinchenko, Rena A.
Afiliação
  • Marakhonov AV; Research Centre for Medical Genetics, Moscow, Russia. marakhonov@generesearch.ru.
  • Konovalov FA; Moscow Institute of Physics and Technology, Dolgoprudny, Russia. marakhonov@generesearch.ru.
  • Makaov AK; Laboratory of Genetic Epidemiology, Research Centre for Medical Genetics, Moskvorechie St., 1, Moscow, Russian Federation, 115478. marakhonov@generesearch.ru.
  • Vasilyeva TA; Genomed Ltd, Moscow, Russia.
  • Kadyshev VV; Khabez central district hospital, Khabez, Russia.
  • Galkina VA; Research Centre for Medical Genetics, Moscow, Russia.
  • Dadali EL; Research Centre for Medical Genetics, Moscow, Russia.
  • Kutsev SI; Research Centre for Medical Genetics, Moscow, Russia.
  • Zinchenko RA; Research Centre for Medical Genetics, Moscow, Russia.
BMC Med Genomics ; 11(Suppl 1): 8, 2018 02 13.
Article em En | MEDLINE | ID: mdl-29504900
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Nanismo / Microcefalia Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Nanismo / Microcefalia Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article