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M. Kalff-Suske (Martha), A. Wild (Anja), H. Topp (Heinrich), M. Wessling (Martina), E.-M. Jacobsen (Eva-Maria), D. Bornholdt (Dorothea), H. Engel (Henk), H. Heuer (Heike), C.M. Aalfs (Cora), M.G.E.M. Ausems (Margreet), et al. R. Barone (Raffaella), A. Herzog (Andre), P. Heutink (Peter), T. Homfray (Tessa), G. Gillessen-Kaesbach (Gabriele), R. König (Rainer), J. Kunze (Jürgen), P. Meinecke (Peter), D. Müller (Dominik), R. Rizzo (Renata), S. Strenge (Sibylle), A. Superti-Furga (Andrea) and K-H. Grzeschik

1999-09-17

Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome

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Human Molecular Genetics , Volume 8 - Issue 9 p. 1769- 1777

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Persistent URL doi.org/10.1093/hmg/8.9.1769, hdl.handle.net/1765/55655
Journal Human Molecular Genetics
Organisation Department of Clinical Chemistry
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Kalff-Suske, M., Wild, A., Topp, H., Wessling, M., Jacobsen, E.-M., Bornholdt, D., … Grzeschik, K.-H. (1999). Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome. Human Molecular Genetics, 8(9), 1769–1777. doi:10.1093/hmg/8.9.1769
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