新发21q22.1q22.2缺失，包括RUNX1，酷似先天性感染。 - Suppr

De Novo 21q22.1q22.2 deletion including RUNX1 mimicking a congenital infection.

作者信息

Thevenon Julien, Callier Patrick, Thauvin-Robinet Christel, Mejean Nathalie, Falcon-Eicher Sylvie, Maynadie Marc, de Maistre Emmanuel, Bidot Samuel, Huet Frédéric, Beri-Dexheimer Mylène, Jonveaux Philippe, Mugneret Francine, Faivre Laurence

出版信息

Am J Med Genet A. 2011 Jan;155A(1):126-9. doi: 10.1002/ajmg.a.33809.

DOI:10.1002/ajmg.a.33809

PMID:21204219

Abstract

摘要

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De Novo 21q22.1q22.2 deletion including RUNX1 mimicking a congenital infection.

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