Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC

American Journal of Medical Genetics

Volumn 140 A, Issue 1, 2006, Pages 46-51

  Liehr, Thomas ^a   Starke, Heike ^a   Senger, Gabriele ^b   Melotte, Cindy ^c   Weise, Anja ^a   Vermeesch, Joris Robert ^c  

^a Institut fur Humangenetik und Anthropologie   (Germany)

^b Praxis f Med Genetik und Gynäkologie   (Germany)

^c UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Array CGH; Chromosome 5; Chromosome 6; Molecular cytogenetics; Small supernumerary marker chromosomes (sSMC)

Indexed keywords

DNA;

ARTICLE; CASE REPORT; CHROMOSOME 20; CHROMOSOME 6; CHROMOSOME 6P; CHROMOSOME 6Q; CHROMOSOME BREAKAGE; CHROMOSOME MICRODISSECTION; CHROMOSOME PAINTING; CLINICAL FEATURE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPE; MARKER CHROMOSOME; PRIORITY JOURNAL; REVERSE CHROMOSOME PAINTING; SMALL SUPERNUMERARY MARKER CHROMOSOME; SUPERNUMERARY CHROMOSOME;

BASE SEQUENCE; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME DISORDERS; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN, PAIR 6; FEMALE; GENOME, HUMAN; HUMANS; KARYOTYPING; MOLECULAR SEQUENCE DATA; NUCLEIC ACID HYBRIDIZATION;

EID: 30144435732     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31048     Document Type: Article

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