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American Journal of Medical Genetics|March 1, 1990
DNA polymerase alpha defect in the N syndromeK M Floy, R O Hess, L F MeisnerAmerican Journal of Medical Genetics. Supplement|January 1, 1987
Apparent Prader-Willi phenotype in a woman with ring chromosome 9R O Hess, L F MeisnerAmerican Journal of Medical Genetics. Supplement|January 1, 1987
Updating the N syndrome: occurrence of lymphoid malignancy and possible association with an increased rate of chromosome breakageR O Hess, G R Hafez, L F MeisnerIn Vitro|December 1, 1984
Synergistic effect of TPA and T-cell mitogens in nonmammalian vertebratesJ E Wiley, L F MeisnerThe Journal of Urology|January 1, 1991
Adenocarcinoma of the prostate in a 41-year-old man with XXY karyotype and chronic lymphocytic leukemia: report of a caseE J Pienkos, L F MeisnerAmerican Journal of Medical Genetics|May 1, 1991
Hereditary hypotrichosis of the scalpR O Hess, H UnoCancer Genetics and Cytogenetics|December 1, 1987
Mechanisms in cyclophosphamide induction of cytogenetic damage in human lymphocyte culturesL M Sargent, B Roloff, L F MeisnerAmerican Journal of Diseases of Children (1960)|November 1, 1983
'Expanded' Prader-Willi syndrome in a boy with an unusual 15q chromosome deletionR M Pauli, L F Meisner, R J SzmandaPediatric Pathology|January 1, 1990
Chromosomal instability in hereditary tyrosinemia type IE Gilbert-Barness, L A Barness, L F MeisnerActa Cytologica|July 1, 1977
Mechanisms of chromatid breakage in human lymphocyte culturesL F Meisner, T W Chuprevich, S L InhornPageof 6