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Autor:
Klara Flipsen-ten Berg, P F Ron Hochstenbach, Martin Poot, Marc J. Eleveld, Frits A. Beemer, Peter M. van Hasselt, Suzanne E van der Wijst, Monique A. M. J. de Vroede, Frans A. Hol
Publikováno v:
European Journal of Human Genetics, 15, 11, pp. 1132-8
European Journal of Human Genetics, 15, 1132-8
European Journal of Human Genetics, 15, 1132-8
Contains fulltext : 36655.pdf (Publisher’s version ) (Closed access) The Wolf-Hirschhorn syndrome (WHS (MIM 194190)), which is characterized by growth delay, mental retardation, epilepsy, facial dysmorphisms, and midline fusion defects, shows exten