Detection of monosomy 7 in bone marrow by fluorescence in situ hybridization: A study of Fanconi anemia patients and review of the literature

Cancer Genetics and Cytogenetics

Volumn 109, Issue 2, 1999, Pages 154-160

  Thurston, Virginia C ^a   Ceperich, Tina M ^b   Vance, Gail H ^a   Heerema, Nyla A ^b  

^a INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b Wayne Hughes Institute   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ACUTE LEUKEMIA; ADULT; ANEMIA; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BONE MARROW CELL; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; FANCONI ANEMIA; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; INFANT; KARYOTYPE; MONOSOMY 7; PRIORITY JOURNAL;

ADOLESCENT; ADULT; BONE MARROW; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 7; FANCONI ANEMIA; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; MIDDLE AGED; MONOSOMY; REFERENCE VALUES; SENSITIVITY AND SPECIFICITY;

EID: 0033064508     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(98)00167-8     Document Type: Article

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