Transient myeloproliferative disorder in a phenotypically normal infant with i(21q) mosaicism

Cancer Genetics and Cytogenetics

Volumn 136, Issue 2, 2002, Pages 138-140

  Wu, Shi Qi ^a   Loh, Kwan Tien ^b   Chen, Xiao Rong ^b   Joo, Wan Jong ^b   Mascarenhas, Leo ^a  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^b ProGene   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PHYTOHEMAGGLUTININ; PRIMER DNA;

ANAMNESIS; ARTICLE; ARTIFICIAL VENTILATION; BLOOD; CASE REPORT; CESAREAN SECTION; CHROMOSOME 21Q; CHROMOSOME ANALYSIS; CHROMOSOME MOSAICISM; CLINICAL FEATURE; COMORBIDITY; DISEASE COURSE; EXCHANGE BLOOD TRANSFUSION; FETUS DISTRESS; FETUS HYDROPS; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; HEMATOLOGICAL PARAMETERS; HUMAN; HUMAN TISSUE; HYPERBILIRUBINEMIA; IMMUNOPHENOTYPING; INFANT; ISOCHROMOSOME; LEUKOCYTE COUNT; LEUKOCYTOSIS; LIVER BIOPSY; LIVER FIBROSIS; MALE; MYELOPROLIFERATIVE DISORDER; PHENOTYPE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; REMISSION; THROMBOCYTE COUNT;

CHROMOSOMES, HUMAN, PAIR 21; HUMANS; INFANT, NEWBORN; ISOCHROMOSOMES; MALE; MOSAICISM; MYELOPROLIFERATIVE DISORDERS;

EID: 0037101581     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(02)00518-6     Document Type: Article

References (8)

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