Výpis publikací

VONDRÁČEK, Petr, Lenka FAJKUSOVÁ, Markéta HERMANOVÁ, Zdenka BÁLINTOVÁ, Pavel SEEMAN, Radim MAZANEC, Eva ZAPLETALOVÁ a Petr BRABEC. New Perspectives in the Treatment of Inherited Neuromuscular Disorders: Innovative Ideas for the Third Millenium. In Focus on Birth Defects Research. 1. vyd. New York: Janet V. Engels (Ed.), Nova Science Publishers, Inc., 2006, s. 161-184. Focus on Birth Defects Research, 1. ISBN 1-59454-959-1.

FAJKUSOVÁ, Lenka a Jana VOJTOVÁ. Role of alternative splicing in the human dystrophin gene. Australia, 2003.

FAJKUSOVÁ, Lenka, Miroslava TVRDÍKOVÁ, Zdeněk LUKÁŠ a Jiří FAJKUS. Analysis of dystrophin mRNA in patients with DMD,BMD and XLDC. In European Journal of Human Genetics. Vienna: nature publishing group, 2001, s. 310.

FAJKUSOVÁ, Lenka, Zdeněk LUKÁŠ, Miroslava TVRDÍKOVÁ, Viera KUHROVÁ, Jiří HÁJEK a Jiří FAJKUS. Novel dystrophin mutations revealed by analysis of dystrophin mRNA: alternative splicing suppresses the phenotypic effect of a nonsense mutation. Neuromuscular Disordes. Amsterdam: Elsevier Science, 2001, roč. 11, č. 2, s. 133-138. ISSN 0960-8966.