Localization by fish of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p)

Genetic Counseling

Volumn 9, Issue 3, 1998, Pages 215-221

  Petit, P ^a,c   Devriendt, K ^a   Vermeesch, J R ^a   Meireleire, J ^b   Fryns, J P ^a  

^a University Hospital Gasthuisberg   (Belgium)

^b MPI Gielsbos   (Belgium)

^c CENTER FOR HUMAN GENETICS   (Belgium)

Author keywords

Centric fission; Chromosomes 9 and 11; Isochromosome; Trisomy 9p

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CENTROMERE; CHROMOSOME 11; CHROMOSOME 4; CHROMOSOME 9; CHROMOSOME BANDING PATTERN; CHROMOSOME BREAKAGE; CHROMOSOME TRANSLOCATION 9; CLINICAL FEATURE; CYTOGENETICS; DNA PROBE; DNA SEQUENCE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; ISOCHROMOSOME; KARYOTYPE 46,XX; MENTAL DEFICIENCY; OLIGONUCLEOTIDE PROBE; PARTIAL TRISOMY 9; RECIPROCAL CHROMOSOME TRANSLOCATION; TELOMERE;

ADULT; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MENTAL RETARDATION; TELOMERE; TRANSLOCATION, GENETIC; TRISOMY;

EID: 0031725384     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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