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NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemia

Cancer research (Chicago, Ill.), 1998-10, Vol.58 (19), p.4269-4273

1998

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Association of Germline p53 Mutation With MLL Segmental Jumping Translocation in Treatment-Related Leukemia

Blood, 1998-06, Vol.91 (12), p.4451-4456

1998

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The t(14;21)(q11.2;q22) Chromosomal Translocation Associated with T-Cell Acute Lymphoblastic Leukemia Activates the BHLHB1 Gene

Proceedings of the National Academy of Sciences - PNAS, 2000-03, Vol.97 (7), p.3497-3502

2000

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Mechanisms of MLL gene rearrangement: site-specific DNA cleavage within the breakpoint cluster region is independent of chromosomal context

Human molecular genetics, 2001-10, Vol.10 (22), p.2481-2491

2001

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Chromosome mapping and organization of the human beta-galactoside alpha 2,6-sialyltransferase gene. Differential and cell-type specific usage of upstream exon sequences in B-lymphoblastoid cells

The Journal of biological chemistry, 1993-02, Vol.268 (6), p.4355-4361

1993

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A Chromosome 11 YAC Library

Genomics (San Diego, Calif.), 1993-06, Vol.16 (3), p.580-585

1993

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Rhabdomyosarcoma of the cervix in sisters with review of the literature

Gynecologic oncology, 2005-12, Vol.99 (3), p.742-748

2005

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A t(11;12) 11q23 leukemic breakpoint that disrupts the MLL Gene

Genes chromosomes & cancer, 1993-05, Vol.7 (1), p.28-31

1993

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Tetrasomy of chromosome 8: An interesting and rare cytogenetic phenomenon in acute nonlymphocytic leukemia

Cancer genetics and cytogenetics, 1987-08, Vol.27 (2), p.269-271

1987

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Chromosome mapping and organization of the human β-galactoside α2,6-sialyltransferase gene : differential and cell-type specific usage of upstream exon sequences in B-lymphoblastoid cells

The Journal of biological chemistry, 1993-02, Vol.268 (6), p.4355-4361

1993

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Cytogenetic study of maturing granulocytes in bone marrow of patients with acute myelogenous leukemia

Leukemia, 1990-04, Vol.4 (4), p.297-301

1990

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Insertion of MLL sequences into chromosome band 5q31 results in an MLL-AF5Q31 fusion and is a rare but recurrent abnormality associated with infant leukemia

Genes chromosomes & cancer, 2003-07, Vol.37 (3), p.326-331

2003

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A uterine leiomyoma showing both t(12;14) and del(7) abnormalities

Cancer genetics and cytogenetics, 1989-02, Vol.37 (2), p.157-161

1989

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Continued cell cycling ability of HL-60 cells following 3HaraC incorporation: A combination of “double-labeling” and sister chromatid analysis

Cancer genetics and cytogenetics, 1987-08, Vol.27 (2), p.311-318

1987

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Translocation t(1;22) in congenital acute megakaryocytic leukemia

Cancer genetics and cytogenetics, 1988-09, Vol.34 (2), p.277-280

1988

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t(y;18) in acute myeloblastic leukemia FAB type M2

Cancer genetics and cytogenetics, 1986-08, Vol.22 (4), p.367-368

1986

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Mapping of ribosomal protein S3 and internally nested snoRNA U15A gene to human chromosome 11q13.3–q13.5

Genomics (San Diego, Calif.), 1995-01, Vol.25 (2), p.577-580

1995

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Recurrent involvement of 11q13 in acute nonlymphocytic leukemia

Cancer genetics and cytogenetics, 1987-06, Vol.26 (2), p.351-354

1987

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A t(1;11) in acute nonlymphocytic leukemia FAB type M4

Cancer genetics and cytogenetics, 1987, Vol.24 (1), p.181-183

1987

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Translocation t(6;9)(p23;q34) in acute nonlymphocytic leukemia: Two new patients without increased bone marrow basophils

Cancer genetics and cytogenetics, 1988, Vol.32 (1), p.153-155

1988

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Trisomy 4: an entity within acute non-lymphocytic leukemia

Cancer genetics and cytogenetics, 1987, Vol.26 (1), p.117-125

1987

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Translocation t(6;9)(p22.3;q34) in myelodysplatic syndrome-refractory anemia with excess blasts

Cancer genetics and cytogenetics, 1987, Vol.29 (1), p.135-138

1987

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A t(11;21)(q13;q22) in Ph-positive chronic myelogenous leukemia

Cancer genetics and cytogenetics, 1988-04, Vol.31 (2), p.187-191

1988

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Complex cytogenetic changes in Ph-negative chronic myelogenous leukemia

Cancer genetics and cytogenetics, 1988-04, Vol.31 (2), p.241-245

1988

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Translocation t(6;9)(p23;q34) in acute nonlymphocytic leukemia. Two new patients without increased bone marrow basophils

Cancer genetics and cytogenetics, 1988, Vol.32 (1), p.153-155

1988

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NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemia

Association of Germline p53 Mutation With MLL Segmental Jumping Translocation in Treatment-Related Leukemia

The t(14;21)(q11.2;q22) Chromosomal Translocation Associated with T-Cell Acute Lymphoblastic Leukemia Activates the BHLHB1 Gene

Mechanisms of MLL gene rearrangement: site-specific DNA cleavage within the breakpoint cluster region is independent of chromosomal context

Chromosome mapping and organization of the human beta-galactoside alpha 2,6-sialyltransferase gene. Differential and cell-type specific usage of upstream exon sequences in B-lymphoblastoid cells

A Chromosome 11 YAC Library

Rhabdomyosarcoma of the cervix in sisters with review of the literature

A t(11;12) 11q23 leukemic breakpoint that disrupts the MLL Gene

Tetrasomy of chromosome 8: An interesting and rare cytogenetic phenomenon in acute nonlymphocytic leukemia

Chromosome mapping and organization of the human β-galactoside α2,6-sialyltransferase gene : differential and cell-type specific usage of upstream exon sequences in B-lymphoblastoid cells

Cytogenetic study of maturing granulocytes in bone marrow of patients with acute myelogenous leukemia

Insertion of MLL sequences into chromosome band 5q31 results in an MLL-AF5Q31 fusion and is a rare but recurrent abnormality associated with infant leukemia

A uterine leiomyoma showing both t(12;14) and del(7) abnormalities

Continued cell cycling ability of HL-60 cells following 3HaraC incorporation: A combination of “double-labeling” and sister chromatid analysis

Translocation t(1;22) in congenital acute megakaryocytic leukemia

t(y;18) in acute myeloblastic leukemia FAB type M2

Mapping of ribosomal protein S3 and internally nested snoRNA U15A gene to human chromosome 11q13.3–q13.5

Recurrent involvement of 11q13 in acute nonlymphocytic leukemia

A t(1;11) in acute nonlymphocytic leukemia FAB type M4

Translocation t(6;9)(p23;q34) in acute nonlymphocytic leukemia: Two new patients without increased bone marrow basophils

Trisomy 4: an entity within acute non-lymphocytic leukemia

Translocation t(6;9)(p22.3;q34) in myelodysplatic syndrome-refractory anemia with excess blasts

A t(11;21)(q13;q22) in Ph-positive chronic myelogenous leukemia

Complex cytogenetic changes in Ph-negative chronic myelogenous leukemia

Translocation t(6;9)(p23;q34) in acute nonlymphocytic leukemia. Two new patients without increased bone marrow basophils

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