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Myotilin is mutated in limb girdle muscular dystrophy 1A

Human molecular genetics, 2000-09, Vol.9 (14), p.2141-2147

2000

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Clinical Significance of the BCR-ABL Fusion Gene in Adult Acute Lymphoblastic Leukemia: A Cancer and Leukemia Group B Study (8762)

Blood, 1992-12, Vol.80 (12), p.2983-2990

1992

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Cytogenetic and Molecular Delineation of the Smallest Commonly Deleted Region of Chromosome 5 in Malignant Myeloid Diseases

Proceedings of the National Academy of Sciences - PNAS, 1993-06, Vol.90 (12), p.5484-5488

1993

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Human mortalin (HSPA9) : a candidate for the myeloid leukemia tumor suppressor gene on 5q31

Leukemia, 2000-12, Vol.14 (12), p.2128-2134

2000

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Cytogenetic and molecular diagnosis of chromosome 5 deletions in myelodysplasia

British journal of haematology, 2000-09, Vol.110 (4), p.847-855

2000

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Detection of bcr-abl Fusion in Chronic Myelogeneous Leukemia by in Situ Hybridization

Science (American Association for the Advancement of Science), 1990-10, Vol.250 (4980), p.559-562

1990

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The first intron in the human c-abl gene is at least 200 kilobases long and is a target for translocations in chronic myelogenous leukemia

Molecular and Cellular Biology, 1987-09, Vol.7 (9), p.3231-3236

1987

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Detection of numerical chromosomal abnormalities in neoplastic hematopoietic cells by in situ hybridization with a chromosome-specific probe

The American journal of pathology, 1990-01, Vol.136 (1), p.131-139

1990

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Polymerase chain reaction-based diagnosis of Del(5q) in acute myeloid leukemia and myelodysplastic syndrome identifies a minimal deletion interval

Blood, 1996-10, Vol.88 (7), p.2665-2670

1996

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Value of molecular monitoring during the treatment of chronic myeloid leukemia: a Cancer and Leukemia Group B study

Journal of clinical oncology, 1997-01, Vol.15 (1), p.26-36

1997

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Human APC gene expression in rodent colonic epithelium in vivo using liposomal gene delivery

Human molecular genetics, 1994-11, Vol.3 (11), p.2005-2010

1994

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Molecular genetics improves the management of hereditary non-polyposis colorectal cancer

South African medical journal, 2000-07, Vol.90 (7), p.709-714

2000

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Unexpected Heterogeneity of BCR-ABL Fusion mRNA Detected by Polymerase Chain Reaction in Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia

Proceedings of the National Academy of Sciences - PNAS, 1989-06, Vol.86 (11), p.4259-4263

1989

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A novel transcriptional suppressor located within a downstream intron of the BCR gene

The Journal of biological chemistry, 1994-04, Vol.269 (14), p.10820-10829

1994

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Evidence for the Involvement of GM-CSF and FMS in the Deletion (5q) in Myeloid Disorders

Science (American Association for the Advancement of Science), 1986-02, Vol.231 (4741), p.984-987

1986

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Localization of gelsolin proximal to ABL on chromosome 9

American journal of human genetics, 1988-04, Vol.42 (4), p.565-572

1988

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The role of molecular techniques in the clinical management of leukemia: Lessons from the philadelphia chromosome

Cancer, 1992-09, Vol.70 (S4), p.1695-1700

Westbrook, Carol A.

1992

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A Radiation Hybrid Breakpoint Map of the Acute Myeloid Leukemia (AML) and Limb-Girdle Muscular Dystrophy 1A (LGMD1A) Regions of Chromosome 5q31 Localizing 122 Expressed Sequences

Genomics (San Diego, Calif.), 1999-04, Vol.57 (1), p.24-35

1999

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A novel nuclear protein, 5qNCA (LOC51780) is a candidate for the myeloid leukemia tumor suppressor gene on chromosome 5 band q31

Oncogene, 2001-10, Vol.20 (47), p.6946-6954

2001

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Relapse after interferon alfa-2b therapy for hairy-cell leukemia: analysis of prognostic variables

Journal of clinical oncology, 1988-11, Vol.6 (11), p.1714-1721

1988

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Immunomagnetic separation can enrich fixed solid tumors for epithelial cells

The American journal of pathology, 1996-01, Vol.148 (1), p.95-104

1996

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Use of a CEPH Meiotic Breakpoint Panel to Refine the Locus of Limb-Girdle Muscular Dystrophy Type 1A (LGMD1A) to a 2-Mb Interval on 5q31

Genomics (San Diego, Calif.), 1998-12, Vol.54 (2), p.250-255

1998

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c-src is Consistently Conserved in the Chromosomal Deletion (20q) Observed in Myeloid Disorders

Proceedings of the National Academy of Sciences - PNAS, 1985-10, Vol.82 (19), p.6692-6696

1985

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Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy

American journal of human genetics, 1995-12, Vol.57 (6), p.1371-1376

1995

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Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy

Journal of medical genetics, 1998-04, Vol.35 (4), p.305-308

1998

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