Syndromic non-compaction of the left ventricle: Associated chromosomal anomalies

Clinical Genetics

Volumn 84, Issue 4, 2013, Pages 362-367

  Digilio, Mc ^a   Bernardini, L ^b   Gagliardi, Mg ^a   Versacci, P ^c   Baban, A ^a   Capolino, R ^a   Dentici, Ml ^a   Roberti, Mc ^a   Angioni, A ^a   Novelli, A ^b   Marino, B ^c   Dallapiccola, B ^a  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^b CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

^c SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

1p36 deletion; 22q11.2 deletion; Cardiomyopathy; Chromosomal anomaly; Non compaction left ventricle

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME INVERSION; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HEART LEFT VENTRICLE; HUMAN; INCONTINENTIA PIGMENTI; INFANT; KARYOTYPE 45,X; KARYOTYPE 46,XX; MAJOR CLINICAL STUDY; MALE; PREVALENCE; PRIORITY JOURNAL; ROBERTSONIAN CHROMOSOME TRANSLOCATION; VENTRICULAR NONCOMPACTION;

ROBERTSONIA;

1P36 DELETION; 22Q11.2 DELETION; CARDIOMYOPATHY; CHROMOSOMAL ANOMALY; NON-COMPACTION LEFT VENTRICLE;

ADOLESCENT; ADULT; CARDIOMYOPATHIES; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; COMPARATIVE GENOMIC HYBRIDIZATION; ECHOCARDIOGRAPHY, DOPPLER; ELECTROCARDIOGRAPHY; FEMALE; HEART VENTRICLES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; KARYOTYPE; MALE; SYNDROME; YOUNG ADULT;

EID: 84883830157     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/cge.12069     Document Type: Article

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