Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome.
| Autor: | Schell, Ute, Hehr, Andreas, Feldman, George J., Robin, Nathaniel H., Zackai, Elaine H., de Die-Smulders, Christine, Viskochil, David H., Stewart, Janet M., Wolff, Gerhard, Ohashi, Hirofumi, Price, R. Arlen, Cohen, M.Michael, Muenke, Maximilian |
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| Zdroj: | Human Molecular Genetics; Mar1995, Vol. 4 Issue 3, p323-328, 6p |
| Databáze: | Complementary Index |
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