Terminal deletion of Xp22.3 associated with contiguous gene syndrome: Léri-Weill dyschondrosteosis, developmental delay, and ichthyosis. - Suppr | 超能文献

Terminal deletion of Xp22.3 associated with contiguous gene syndrome: Léri-Weill dyschondrosteosis, developmental delay, and ichthyosis.

作者信息

Vassal H, Medeira A, Cordeiro I, Santos H G, Castedo S, Saraiva C, da Silva P M, Monteiro C

出版信息

Am J Med Genet. 2001 Apr 1;99(4):331-4. doi: 10.1002/1096-8628(20010401)99:4<331::aid-ajmg1175>3.0.co;2-w.

DOI:10.1002/1096-8628(20010401)99:4<331::aid-ajmg1175>3.0.co;2-w

Abstract

摘要

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