Diagnosis of 22q11 deletion and duplication in congenital heart disease by multiplex ligation-dependent probe amplification

Chinese Journal of Contemporary Pediatrics

Volumn 11, Issue 11, 2009, Pages 892-896

  Yang, Yue Hua ^a   Hu, Ya Li ^a   Zhu, Xiang Yu ^a   Mo, Xu Ming ^a   Wang, Dong Jin ^a   Yao, Jin Cui ^a   Sheng, Min ^a   Zhu, Hai Yan ^a   Li, Jie ^a   Ru, Tong ^a   Wang, Zhi Qun ^a  

^a NANJING MEDICAL UNIVERSITY   (China)

Author keywords

22q11 deletion; 22q11 duplication; Child; Congenital heart disease; Fetus; Multiplex ligation dependent probe amplification

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 10; CHROMOSOME 17; CHROMOSOME 22; CHROMOSOME 8; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CLINICAL ARTICLE; CONGENITAL HEART DISEASE; DOWN SYNDROME; FALLOT TETRALOGY; HEART VENTRICLE SEPTUM DEFECT; HUMAN; KARYOTYPE; KARYOTYPING; MOSAICISM; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; PULMONARY VALVE STENOSIS; TRISOMY 8;

ADOLESCENT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; GENE DUPLICATION; HEART DEFECTS, CONGENITAL; HUMANS; INFANT, NEWBORN; MALE; NUCLEIC ACID AMPLIFICATION TECHNIQUES;

EID: 71049158011     PISSN: 10088830     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (12)

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