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A common FGFR3 mutation functions as a diagnostic marker for achondroplasia-group disorders in the Japanese population
Yoshito Matsui, Tomoatsu Kimura, Noriyuki Tsumaki, Haruhiko Nakahara, Nobuhito Araki, Natsuo Yasui, Takahiro OchiVolume:
1
Year:
1996
Language:
english
Pages:
6
DOI:
10.1007/bf02348804
File:
PDF, 668 KB
english, 1996