Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: Case report

Molecular Cytogenetics

Volumn 2, Issue 1, 2009, Pages

  De Vree, Paula J P ^a   Simon, Marleen E H ^a   Van Dooren, Marieke F ^a   Stoevelaar, Gerda H T ^a   Hilkmann, José T W ^a   Rongen, Michel A ^a   Huijbregts, Gido C M ^a   Verkerk, Annemieke J M H ^a   Poddighe, Pino J ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; CHROMOSOME 1; CHROMOSOME 10; CHROMOSOME 11; CHROMOSOME 13; CHROMOSOME 15; CHROMOSOME 18; CHROMOSOME 5; CHROMOSOME 9; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; COMPLEX CHROMOSOME REARRANGEMENT; CYTOGENETICS; FLUORESCENCE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC PROCEDURES; GENOTYPE; HUMAN; HUMAN CELL; KARYOTYPE; MALE; MULTICOLOR FLUORESCENCE IN SITU HYBRIDIZATION; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; PHENOTYPE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 69049083541     PISSN: None     EISSN: 17558166     Source Type: Journal    
DOI: 10.1186/1755-8166-2-15     Document Type: Article

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