Clinical Application of Microarray-Based Molecular Cytogenetics: An Emerging New Era of Genomic Medicine

Journal of Pediatrics

Volumn 155, Issue 3, 2009, Pages 311-317

  Li, Marilyn M ^a   Andersson, Hans C ^a  

^a TULANE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MIDOSTAURIN;

ACQUIRED IMMUNE DEFICIENCY SYNDROME; ACUTE GRANULOCYTIC LEUKEMIA; ALZHEIMER DISEASE; ARTICLE; AUTISM; AUTOSOMAL DOMINANT DISORDER; BACTERIAL INFECTION; BREAST CANCER; CANCER GENETICS; CANCER SUSCEPTIBILITY; CHILDHOOD LEUKEMIA; CHROMOSOME 3Q; COLORECTAL CANCER; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL MALFORMATION; CROHN DISEASE; CYTOGENETICS; DEVELOPMENTAL DISORDER; EARLY DIAGNOSIS; FAMILIAL CANCER; FAMILIAL DISEASE; GENE LOCUS; GENE MUTATION; GENETIC DISORDER; GENETIC SUSCEPTIBILITY; GENOMICS; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS INFECTION; MENTAL RETARDATION MALFORMATION SYNDROME; MICROARRAY ANALYSIS; MULTIPLE MALFORMATION SYNDROME; MULTIPLE MYELOMA; PARKINSON DISEASE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SYNDROME CHARGE; TUMOR SUPPRESSOR GENE;

AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; CONGENITAL ABNORMALITIES; CYTOGENETICS; DEVELOPMENTAL DISABILITIES; FORECASTING; GENOMICS; GENOTYPE; HUMANS; MENTAL RETARDATION; MUTATION; NEOPLASMS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PHENOTYPE;

EID: 69249234781     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpeds.2009.04.001     Document Type: Article

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