论文信息 - A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly. - 字舞流文

A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly.

U. Müller | D. Steinberger | H. Collmann | B. Schmalenberger | Daniela Steinberger | Hartmut Collmann | Bernhard Schmalenberger | Ulrich Muller | U. Miller