Array based characterization of a terminal deletion involving chromosome subband 15q26.2: An emerging syndrome associated with growth retardation, cardiac defects and developmental delay

BMC Medical Genetics

Volumn 9, Issue , 2008, Pages

  Davidsson, Josef ^a   Collin, Anna ^a   Björkhem, Gudrun ^a   Soller, Maria ^a  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE; DIGITALIS; PROSTAGLANDIN;

AORTA COARCTATION; ARTICLE; CASE REPORT; CHROMOSOME 15Q; CHROMOSOME ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; DEVELOPMENTAL DISORDER; DICENTRIC CHROMOSOME; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MAPPING; GROWTH RETARDATION; HEART DISEASE; HEART VENTRICLE SEPTUM DEFECT; HUMAN; MALE; METAPHASE; MOLECULAR GENETICS; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRESCHOOL CHILD; SUPRAVENTRICULAR TACHYCARDIA; ADULT; CHROMOSOME 15; CHROMOSOME BANDING PATTERN; CHROMOSOME DELETION; CHROMOSOME PAINTING; CONGENITAL HEART MALFORMATION; FEMALE; GENETICS; GROWTH DISORDER; INFANT; KARYOTYPING; SYNDROME;

ADULT; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN, PAIR 15; DEVELOPMENTAL DISABILITIES; FEMALE; GROWTH DISORDERS; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; METAPHASE; SYNDROME;

EID: 39349116291     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-9-2     Document Type: Article

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