De novo structural chromosomal imbalances: Molecular cytogenetic characterization of partial trisomies

Cytogenetic and Genome Research

Volumn 114, Issue 3-4, 2006, Pages 342-350

  Dufke, A ^a   Singer, S ^a   Borell Kost, S ^a   Stotter M ^a   Pflumm, D A ^a   Mau Holzmann, U A ^a   Starke, H ^b   Mrasek, K ^b   Enders, H ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

VALPROIC ACID; MICROSATELLITE DNA;

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 10Q; CHROMOSOME 12P; CHROMOSOME 17P; CHROMOSOME 18Q; CHROMOSOME ANALYSIS; CHROMOSOME BANDING PATTERN; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME INVERSION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; DISEASE SEVERITY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE 46,XX; MALE; MENTAL DEFICIENCY; MOLECULAR PROBE; PARTIAL TRISOMY; PARTIAL TRISOMY 10; PETIT MAL; PRIORITY JOURNAL; SPECTRAL KARYOTYPING; STRUCTURAL CHROMOSOME ABERRATION; CHROMOSOME 10; CHROMOSOME 12; CHROMOSOME 15; CHROMOSOME 18; CHROMOSOME ABERRATION; CHROMOSOME PAINTING; GENE DELETION; GENE REARRANGEMENT; GENETICS; TRISOMY;

CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 18; CYTOGENETIC ANALYSIS; FEMALE; GENE REARRANGEMENT; HUMANS; MICROSATELLITE REPEATS; SEQUENCE DELETION; TRISOMY;

EID: 33748468773     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000094224     Document Type: Article

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