Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2
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R. Weksberg | J. Opitz | J. Allanson | B. Burton | R. Laxová | M. Guion-Almeida | M. Muenke | R. Price | N. Robin | H. Mitchell | C. Leonard | L. Leichtman | Rick A. Martin | K. Aleck | G. Feldman | K. Josephson | Adam L. Aronson | Adam L. Aronson | J. Opitz