7例伴有22q11.2染色体缺失的凯勒心脏颜面综合征新病例，包括1例家族性病例。 - Suppr

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超能文献

Seven new cases of Cayler cardiofacial syndrome with chromosome 22q11.2 deletion, including a familial case.

作者信息

Bawle E V, Conard J, Van Dyke D L, Czarnecki P, Driscoll D A

出版信息

Am J Med Genet. 1998 Oct 12;79(5):406-10. doi: 10.1002/(sici)1096-8628(19981012)79:5<406::aid-ajmg18>3.0.co;2-v.

DOI:10.1002/(sici)1096-8628(19981012)79:5<406::aid-ajmg18>3.0.co;2-v

PMID:9779813

Abstract

摘要

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