M.J. Pettenati

The human cornea has a high incidence of acquired chromosome abnormalities

M.J. Pettenati, Andrew J. Sweatt, Patrick E. Lantz et al. · Human Genetics · 1997 · 275 citations

Ophthalmology, Cytogenetics, Corneal Dystrophy +9

Identification of a human gene (HCK) that encodes a protein-tyrosine kinase and is expressed in hemopoietic cells.

Nancy Quintrell, R V Lebo, Harold Varmus et al. · Molecular and Cellular Biology · 1987 · 272 citations · Full text

Mixed-phenotype Acute Leukemia, Human Leukemias, Immunology +16

Assignment of the GM-CSF, CSF-1, and FMS Genes to Human Chromosome 5 Provides Evidence for Linkage of a Family of Genes Regulating Hematopoiesis and for Their Involvement in the Deletion (5q) in Myeloid Disorders

Michelle M. Le Beau, M.J. Pettenati, R.S. Lemons et al. · Cold Spring Harbor Symposia on Quantitative Biology · 1986 · 55 citations

Mixed-phenotype Acute Leukemia, Genetics, Genetic Epidemiology +20

Chromosomal localization of the human G-CSF gene to 17q11 proximal to the breakpoint of the t(15;17) in acute promyelocytic leukemia.

Michelle M. Le Beau, R.S. Lemons, John J. Carrino et al. · PubMed · 1987 · 32 citations

Clinical characteristics of patients with <i>de novo</i> acute myeloid leukaemia and isolated trisomy 11: a Cancer and Leukemia Group B study

Kristiina Heinonen, Krzysztof Mrózek, David Lawrence et al. · British Journal of Haematology · 1998 · 29 citations · Full text