Transient QT interval prolongation in an infant with Simpson-Golabi-Behmel syndrome

American Journal of Medical Genetics, Part A

Volumn 152, Issue 9, 2010, Pages 2379-2382

  Gertsch, Emily ^a   Kirmani, Salman ^a   Ackerman, Michael J ^a   Babovic Vuksanovic, Dusica ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BETA ADRENERGIC RECEPTOR BLOCKING AGENT;

CACNA1C GENE; CARDIAC CHANNELOPATHY; CASE REPORT; CLEFT PALATE; CLINICAL FEATURE; DEFIBRILLATOR; DIAGNOSTIC ERROR; ELECTROCARDIOGRAPHY; FETUS; GENE; GENETIC DISORDER; GENETIC SCREENING; GPC3 GENE; HUMAN; INFANT; LETTER; MACROSOMIA; MALE; NEWBORN; PHENOTYPE; PRIORITY JOURNAL; QT PROLONGATION; SIMPSON GOLABI BEHMEL SYNDROME; SINUS BRADYCARDIA; SYNDACTYLY; TIMOTHY SYNDROME;

ABNORMALITIES, MULTIPLE; ARRHYTHMIAS, CARDIAC; ELECTROCARDIOGRAPHY; FAMILY; GIGANTISM; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; LONG QT SYNDROME; MENTAL RETARDATION;

EID: 77956115109     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33561     Document Type: Letter

References (11)

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