SNP array karyotyping allows for the detection of uniparental disomy and cryptic chromosomal abnormalities in MDS/MPD-U and MPD

PLoS ONE

Volumn 2, Issue 11, 2007, Pages

  Gondek, Lukasz P ^a   Dunbar, Andrew J ^a   Szpurka, Hadrian ^a   McDevitt, Michael A ^b   Maciejewski, Jaroslaw P ^a  

^a TAUSSIG CANCER INSTITUTE   (United States)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

JANUS KINASE 2; PRIMER DNA;

ADULT; AGED; ARTICLE; CHROMOSOME 1; CHROMOSOME 11; CHROMOSOME 12; CHROMOSOME 22; CHROMOSOME 9P; CHROMOSOME ABERRATION; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; FEMALE; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC TRANSFORMATION; HOMOZYGOTE; HUMAN; KARYOTYPING; MALE; METAPHASE CHROMOSOME; MUTANT; MYELODYSPLASTIC SYNDROME; MYELOID LEUKEMIA; MYELOPROLIFERATIVE DISORDER; SINGLE NUCLEOTIDE POLYMORPHISM; UNIPARENTAL DISOMY; GENETICS; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION;

BASE SEQUENCE; CHROMOSOME ABERRATIONS; DNA PRIMERS; HUMANS; KARYOTYPING; MYELODYSPLASTIC SYNDROMES; MYELOPROLIFERATIVE DISORDERS; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; UNIPARENTAL DISOMY;

EID: 43249121366     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0001225     Document Type: Article

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