Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases.
Siitonen, H. Annika; Kopra, Outi; Kääriäinen, Helena; Haravuori, Henna; Winter, Robin M.; Säämänen, Anna-Marja; Peltonen, Leena; Kestilä, Marjo; Human Molecular Genetics, 2003, vol. 12, issue 21, p 2837, ISSN 09646906. ISBN 09646906.

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