Impact of DEL22q11, trisomy 21, and other genetic syndromes on surgical outcome of conotruncal heart defects

Journal of Thoracic and Cardiovascular Surgery

Volumn 138, Issue 3, 2009, Pages

  Michielon, Guido ^a   Marino, Bruno ^a   Oricchio, Gianluca ^a   Digilio, Maria Cristina ^a   Iorio, Fiore ^a   Filippelli, Sergio ^a   Placidi, Silvia ^a   Di Donato, Roberto M ^a  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ALAGILLE SYNDROME; ARTICLE; CANTRELL SYNDROME; CARDIOPULMONARY BYPASS; CHILD; CHILDHOOD MORTALITY; CHROMOSOME 22Q; CHROMOSOME DELETION; CHROMOSOME DELETION 5; CHROMOSOME DUPLICATION; CHROMOSOME TRANSLOCATION; CONGENITAL HEART MALFORMATION; CONOTRUNCAL HEART DEFECT; CONTROLLED STUDY; CYSTIC FIBROSIS; FEMALE; GENETIC DISORDER; GENETIC RISK; GOLDENHAR SYNDROME; HEART SURGERY; HUMAN; INFANT; KABUKI MAKEUP SYNDROME; KLIPPEL FEIL SYNDROME; MAJOR CLINICAL STUDY; MALE; NOONAN SYNDROME; POSTOPERATIVE COMPLICATION; PREOPERATIVE PERIOD; PRESCHOOL CHILD; PRIORITY JOURNAL; REOPERATION; RESIDUAL BRANCHIAL ARCH SYNDROME; RISK ASSESSMENT; SCHOOL CHILD; SURGICAL ANATOMY; SURGICAL TECHNIQUE; SURVIVAL RATE; SURVIVAL TIME; SYNDROME CHARGE; SYNDROME VATER; TORELL SYNDROME; TOWNES BROCKS SYNDROME; TREATMENT OUTCOME; TRISOMY 21; TRISOMY 22; TURNER SYNDROME; WAARDENBURG SYNDROME; WILLIAMS BEUREN SYNDROME;

EID: 68749084593     PISSN: 00225223     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jtcvs.2009.03.009     Document Type: Article

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