Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases.
Siitonen HA; Kopra O; Kääriäinen H; Haravuori H; Winter RM; Säämänen AM; Peltonen L; Kestilä M; Human Molecular Genetics, 2003, vol. 12, issue 21, p 2837, ISSN 09646906. ISBN 09646906.

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