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Cytogenetics and Cell Genetics|January 1, 1997
Mapping FRA11A, a folate-sensitive fragile site in human chromosome band 11q13.3D Perucca-Lostanlen, B K Hecht, A Courseaux, et al.Biomedical Optics Express|July 5, 2021
Complex wavelet filter improves FLIM phasors for photon starved imaging experimentsP Wang, F Hecht, G Ossato, et al.Cancer Genetics and Cytogenetics|November 1, 1981
Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemiaF P Li, F Hecht, B Kaiser-McCaw, et al.Cancer Research|May 15, 1988
Philadelphia chromosome-positive acute lymphoblastic leukemia cell lines without classical breakpoint cluster region rearrangementL Naumovski, R Morgan, F Hecht, et al.Blood|June 1, 1989
Long-term growth of malignant thymocytes in vitroS D Smith, P McFall, R Morgan, et al.Prenatal Diagnosis|May 1, 1988
Prenatal diagnosis of a de novo unbalanced translocation (4p+) following in vitro fertilizationL A Cannizzaro, B K Hecht, H A Bixenman, et al.Cancer Research|October 1, 1996
Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumorsR Shridhar, V Shridhar, X Wang, et al.Human Genetics|July 1, 1986
Telomeric fusion in pre-T-cell acute lymphoblastic leukemiaR Morgan, V Jarzabek, J P Jaffe, et al.American Journal of Human Genetics|November 15, 2000
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndromeJ Fang, S L Dagenais, R P Erickson, et al.Leukemia|September 1, 1989
Association of a mature B cell leukemia with a 4p+ chromosomal abnormality: derivation and characterization of a cell lineT E Gribbin, C K Stein, J S Harrison, et al.Pageof 22