Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery

Cardiology in the Young

Volumn 19, Issue 2, 2009, Pages 179-184

  Hu, Yali ^a   Zhu, Xiangyu ^a   Yang, Yuehua ^b   Mo, Xuming ^d   Sheng, Min ^b   Yao, Jincui ^a   Wang, Dongjing ^c  

^a MEDICAL SCHOOL OF NANJING UNIVERSITY   (China)

^b NANJING MEDICAL UNIVERSITY   (China)

^c THE AFFILIATED DRUM TOWER HOSPITAL OF NANJING UNIVERSITY MEDICAL SCHOOL   (China)

^d CHILDREN S HOSPITAL OF NANJING MEDICAL UNIVERSITY   (China)

Author keywords

22q11 deletion syndrome; Cat eye syndrome; DiGeorge syndrome; Velocardiofacial syndrome

Indexed keywords

ADOLESCENT; ADULT; ANEUPLOIDY; ARTICLE; CHILD; CHROMOSOME 22Q; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CONGENITAL HEART DISEASE; FALLOT TETRALOGY; FEMALE; FETUS; HEART ATRIUM SEPTUM DEFECT; HEART VENTRICLE SEPTUM DEFECT; HUMAN; KARYOTYPING; MAJOR CLINICAL STUDY; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; NEWBORN; NONHUMAN; PHENOTYPE; PULMONARY ARTERY STENOSIS; TRISOMY 21; TRISOMY 8; CELL CULTURE; CHINA; CHROMOSOME 22; CLINICAL TRIAL; COMPARATIVE STUDY; CONGENITAL HEART MALFORMATION; FOLLOW UP; GENE DELETION; GENETICS; HEART SURGERY; INCIDENCE; LYMPHOCYTE; MALE; METHODOLOGY; MIDDLE AGED; MULTICENTER STUDY; NUCLEIC ACID AMPLIFICATION; PATHOLOGY; PREGNANCY; RETROSPECTIVE STUDY; ULTRAVIOLET SPECTROPHOTOMETRY;

DNA;

ADOLESCENT; ADULT; CARDIAC SURGICAL PROCEDURES; CELLS, CULTURED; CHINA; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 22; DNA; FEMALE; FOLLOW-UP STUDIES; GENE DELETION; HEART DEFECTS, CONGENITAL; HUMANS; INCIDENCE; INFANT, NEWBORN; KARYOTYPING; LYMPHOCYTES; MALE; MIDDLE AGED; NUCLEIC ACID AMPLIFICATION TECHNIQUES; PREGNANCY; RETROSPECTIVE STUDIES; SPECTROPHOTOMETRY, ULTRAVIOLET; YOUNG ADULT;

EID: 66149133668     PISSN: 10479511     EISSN: 14671107     Source Type: Journal    
DOI: 10.1017/S1047951109003667     Document Type: Article

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