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Volumn 124, Issue 1-2, 1999, Pages 3-7
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Congenital cardiovascular malformations and chromosomal microdeletions in 22q11.2;Angeborene kardiovaskulare fehlbildungen und chromosomale mikrodeletionen in 22q11.2
a
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Author keywords
[No Author keywords available]
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Indexed keywords
ADOLESCENT;
ADULT;
ARTICLE;
CARDIOVASCULAR MALFORMATION;
CHILD;
CHROMOSOME 22Q;
CHROMOSOME DELETION;
DIGEORGE SYNDROME;
FALLOT TETRALOGY;
FEMALE;
FETUS;
HEART VENTRICLE SEPTUM DEFECT;
HUMAN;
HUMAN CELL;
HUMAN TISSUE;
INCIDENCE;
INFANT;
LUNG ATRESIA;
MAJOR CLINICAL STUDY;
MALE;
NEWBORN;
VELOCARDIOFACIAL SYNDROME;
ANGIOGRAPHY;
CHROMOSOME 22;
COMPARATIVE STUDY;
CONGENITAL HEART MALFORMATION;
CRANIOFACIAL MALFORMATION;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENETICS;
KARYOTYPING;
PRESCHOOL CHILD;
RADIOGRAPHY;
SYNDROME;
ADOLESCENT;
ADULT;
ANGIOGRAPHY;
CHILD;
CHILD, PRESCHOOL;
CHROMOSOME DELETION;
CHROMOSOMES, HUMAN, PAIR 22;
CRANIOFACIAL ABNORMALITIES;
DIGEORGE SYNDROME;
FEMALE;
HEART DEFECTS, CONGENITAL;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
INFANT;
INFANT, NEWBORN;
KARYOTYPING;
MALE;
SYNDROME;
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EID: 0033534195
PISSN: 00120472
EISSN: None
Source Type: Journal
DOI: 10.1055/s-2008-1062601 Document Type: Article |
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Times cited : (12)
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References (11)
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