Mutations in FGFR1 and...

Human Molecular Genetics 1995 Vol. 4; Iss. 3

Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome

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.
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Volume:
4
Year:
1995
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/4.3.323
File:
PDF, 1.95 MB
english, 1995
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