Identification of various MLL gene aberrations that lead to MLL gene mutation in patients with acute lymphoblastic leukemia (ALL) and infants with acute leukemia

Leukemia Research

Volumn 29, Issue 5, 2005, Pages 517-526

  Pais, Anurita ^a   Amare Kadam, Pratibha ^a   Raje, Gauri ^a   Sawant, Manisha ^a   Kabre, Sharayu ^a   Jain, Hemani ^a   Advani, Suresh ^a   Banavali, Shripad ^a  

^a TATA MEMORIAL HOSPITAL   (India)

Author keywords

Acute lymphoblastic leukemia; Conventional karyotyping; FISH; MLL; Southern blotting

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; ADULT; ARTICLE; B LYMPHOCYTE; BLAST CELL; CHILD; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME INSERTION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FREQUENCY ANALYSIS; GENE; GENE FUSION; GENE IDENTIFICATION; GENE MUTATION; HOSPITAL; HUMAN; HUMAN CELL; INCIDENCE; INDIA; INFANT; KARYOTYPING; LEUKOCYTOSIS; MAJOR CLINICAL STUDY; MALE; METAPHASE; MYELOID LYMPHOID LEUKEMIA GENE; PHENOTYPE; PRIORITY JOURNAL; PROGNOSIS; SOUTHERN BLOTTING; STATISTICAL SIGNIFICANCE;

EID: 14744268243     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.leukres.2004.11.016     Document Type: Article

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