Clonality of cell populations in refractory anaemia using combined approach of gene loss and X‐linked restriction fragment length polymorphism‐methylation analyses

Molecular cloning: A laboratory manual

1990 • 85,659 citations

Proposals for the classification of the myelodysplastic syndromes

1982 • 3,616 citations

Molecular cloning of a new transforming gene from a chemically transformed human cell line

1984 • 966 citations

An improved rosetting assay for detection of human T lymphocytes

1974 • 674 citations

Clonal analysis using recombinant DNA probes from the X-chromosome.

1987 • 439 citations

Use of Restriction Fragment Length Polymorphisms to Determine the Clonal Origin of Human Tumors

1985 • 387 citations

Evidence for a multistep pathogenesis of chronic myelogenous leukemia

1981 • 331 citations

Clonal analysis of myelodysplastic syndromes: evidence of multipotent stem cell origin

1989 • 312 citations

Evidence for a multistep pathogenesis of a myelodysplastic syndrome

1984 • 303 citations

A common progenitor for human myeloid and lymphoid cells

1978 • 282 citations

Cloning a selected fragment from a human DNA ‘fingerprint’: isolation of an extremely polymorphic minisatellite

1986 • 243 citations

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

1986 • 233 citations

Expression of the human c-fms proto-oncogene in hematopoietic cells and its deletion in the 5q− syndrome

1985 • 180 citations

Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine-rich island at the 5' end of the gene for phosphoglycerate kinase.

1986 • 164 citations

Clonal studies in the myelodysplastic syndrome using X-linked restriction fragment length polymorphisms

1990 • 135 citations

Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): Correlation with X-inactivation status

1990 • 121 citations

Myelodysplastic syndromes: pathogenesis, functional abnormalities, and clinical implications.

1985 • 105 citations

Monosomy 7 in Granulocytes and Monocytes in Myelodysplastic Syndrome

1987 • 99 citations

Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22

1989 • 92 citations

Multi-allelic RFLP for M27β, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255]

1987 • 69 citations

Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.

1991 • 58 citations

Cytogenetic evidence for involvement of B lymphocytes in acquired idiopathic sideroblastic anemias

1987 • 55 citations

Molecular characterization of chromosome 7 long arm deletions in myeloid disorders

1987 • 48 citations

Human renin gene assigned to chromosome band 1q42 by in situ hybridization

1988 • 19 citations