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Volumn 164, Issue 3, 2014, Pages 9-10
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Genetic testing using array comparative genomic hybridization may benefit newborns with congenital heart disease: Study shows aCGH more effective at detecting potential genetic causes of CHD than other methods
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NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
ARTICLE;
CHROMOSOME IDENTIFICATION;
CLINICAL FEATURE;
COMPARATIVE GENOMIC HYBRIDIZATION;
CONGENITAL HEART DISEASE;
COPY NUMBER VARIATION;
DISEASE SEVERITY;
EMBRYO DEVELOPMENT;
EXOME;
GENE EXPRESSION;
GENETIC SCREENING;
HUMAN;
INCIDENCE;
MUTATIONAL ANALYSIS;
PRIORITY JOURNAL;
SEQUENCE ANALYSIS;
WHOLE EXOME SEQUENCING;
CHROMOSOME ABERRATION;
CHROMOSOME ANALYSIS;
CLINICAL PRACTICE;
FEMALE;
GENETICS;
HEART DEFECTS, CONGENITAL;
HUMAN CHROMOSOME;
MALE;
UTILIZATION;
CHROMOSOME ABERRATIONS;
CHROMOSOMES, HUMAN;
CYTOGENETIC ANALYSIS;
FEMALE;
GENETIC TESTING;
HEART DEFECTS, CONGENITAL;
HUMANS;
MALE;
PHYSICIAN'S PRACTICE PATTERNS;
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EID: 84894244932
PISSN: 15524825
EISSN: 15524833
Source Type: Journal
DOI: 10.1002/ajmg.a.36460 Document Type: Article |
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Times cited : (3)
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References (4)
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