A new case of 8p23.1 deletion including a proposed candidate gene for Cornelia de Lange syndrome without the associated phenotype

被引：0
|
作者：
Ballarati, L. [1 ]
Caselli, R. [1 ]
Recalcati, M. [1 ]
Selicorni, A. [2 ]
Maitz, S. [2 ]
Cereda, A. [2 ]
Valtorta, C. [1 ]
Finelli, P. [3 ]
Larizza, L. [3 ]
Giardino, D. [1 ]
机构：
[1] IRCCS Inst Auxol Italiano, San Giovanni Rotondo, Italy
[2] IRCCS Policlin Milano, Milan, Italy
[3] Univ Milan, I-20122 Milan, Italy
来源：
CHROMOSOME RESEARCH | 2009年 / 17卷
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D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
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页码：196 / 196
页数：1
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