1. E. V. Zaklyazminskaya, V.M. Kozlova, A. V. Polyakov. Germine deletion of the SH2D1A gene in Russian family. // European Journal of Human Genetics. V.12. – S.1 – June 2004. - P0727. - p. 241.
2. Заклязьминская Е.В., Кондратенко И.В., Бологов А.А., Пащенко О.Е., Козлова В.М., Поляков А.В. Этиология и ДНК-диагностика Х-сцепленного лимфопролиферативного синдрома (болезни Дункан).// Медицинская генетика, 2005, т.4, № 11, с.512-515 PDF
3. N.V. Poltavets, M.A. Maschan, I.G. Sermyagina, V.V. Zabnenkova, I.V.Kondratenko, G.A. Novichkova, A.A.Maschan , A.V.Polyakov, Five SH2D1A mutations on 7 chromosomes detected in Russian patients with X-linked lymphoproliferative syndrome (XLP) // 25 Annual meeting of the Histiocyte Society September 15-17, 2009, Bilbao, Spain .
4. N.V.Poltavets, M.A.Maschan, I.G.Sermyagina, A.V.Polyakov, I.V.Kondratenko, A.A.Maschan, G.A.Novichkova, Four SH2D1A mutations on 7 chromosomes detected in Russian patients with X-linked lymphoproliferative syndrome (XLP) // The abstracts of the 41-th European Human Genetics Conference. Vienna, Austria, 23 - 26 May 2009 Europ. J. Hum. Genet., 2009. P12.169, p.347.