Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: Clinical aspects

R. C.M. Hennekam*, M. Tilanus, B. C.J. Hamel, H. Voshart-van Heeren, E. C.M. Mariman, S. E.C. Van Beersum, M. J.H. Van den Boogaard, M. H. Breuning

*Corresponding author for this work

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Biochemistry, Genetics and Molecular Biology