THE USE OF ARRAY CGH IN A COHORT OF ALBANIAN CHILDREN WITH DEVELOPMENT DELAY/INTELLECTUAL DISABILITY, CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES

被引：0

作者：

Babameto-Laku, Anila ^{[1
]}

Roko, Dorina ^{[1
]}

Tabaku, Mirela ^{[1
]}

Bali , Donjeta ^{[2
]}

机构：

[1] Univ Hosp Ctr Mother Teresa, Fac Med, Dept Pediat, Serv Med Genet, Tirana, Albania

[2] Univ Hosp Ctr Mother Teresa, Fac Med, Dept Pediat, Serv Oncohematol, Tirana, Albania

来源：

EUROPEAN JOURNAL OF PEDIATRICS | 2017年 / 176卷 / 11期

关键词：

congenital anomalies; deletion; duplication; intellectual disability; karyotype; microarray comparative genomic hybridization;

D O I：

暂无

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

476

引用

页码：1495 / 1495

页数：1

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