A rare inherited case of 4q deletion detected by GTG and array analyses in a newborn

被引：0
|
作者：
Cobos, Manuela Ariza [1 ]
Miguez, Luz [1 ]
Banos, Francisco [1 ]
Pardo, Victoria [1 ]
Lois, Cristina [1 ]
Martinez, Raquel [2 ]
Macia, Manuel [3 ]
Dominguezi, Fernando [1 ]
机构：
[1] Fdn Publ Galega Med Xen, Prenatal Diagnoses, Santiago De Compostela, Spain
[2] Hosp Cristal Paediat, Orense, Spain
[3] Univ Santiago de Compostela, Hosp Clin, Gynecol, Santiago De Compostela, Spain
来源：
CHROMOSOME RESEARCH | 2011年 / 19卷
关键词：
4q deletion syndrome; Array analyses;
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：
1.P32
引用
收藏
页码：S54 / S54
页数：1
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