Chromosome 4q deletion syndrome: Narrowing the cardiovascular critical region to 4q32.2-q34.3

American Journal of Medical Genetics, Part A

Volumn 158 A, Issue 3, 2012, Pages 635-640

  Xu, Wenbo ^a   Ahmad, Ayesha ^a   Dagenais, Susan ^a   Iyer, Ramaswamy K ^a   Innis, Jeffrey W ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

4q deletion syndrome; Atrial septal defect (ASD); Ventricular septal defect (VSD)

Indexed keywords

15 HYDROXYPROSTAGLANDIN DEHYDROGENASE; BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; DNA; MICRORNA; PROTEIN HAND2; PROTEIN TLL1; TOLLOID METALLOPROTEINASE; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 4Q; CHROMOSOME 4Q DELETION SYNDROME; CHROMOSOME 4Q32.2 Q34.3; CHROMOSOME DELETION 4; CHROMOSOME Q BAND; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL HEART MALFORMATION; DEVELOPMENTAL DISORDER; DNA DETERMINATION; ECHOCARDIOGRAPHY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; HAND2 GENE; HEART ATRIUM SEPTUM DEFECT; HEART VENTRICLE SEPTUM DEFECT; HETEROZYGOSITY; HPGD GENE; HUMAN; INFANT; INTERSTITIAL CHROMOSOME DELETION; MALE; NUCLEOTIDE SEQUENCE; PATENT DUCTUS ARTERIOSUS; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PULMONARY VALVE DISEASE; PULMONARY VALVE INSUFFICIENCY; PULMONARY VALVE STENOSIS; RNA SEQUENCE; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; TLL1 GENE;

CARDIOVASCULAR SYSTEM; CHROMOSOME DELETION; CHROMOSOMES, ARTIFICIAL, BACTERIAL; CHROMOSOMES, HUMAN, PAIR 4; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; GENE DOSAGE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE;

EID: 84863418983     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34425     Document Type: Article

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