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American Journal of Medical Genetics|October 1, 1990
Somatic mosaicism at the Duchenne locusR V Lebo, R K Olney, M S GolbusAmerican Journal of Medical Genetics|September 1, 1993
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by multicolor in situ hybridizationR V Lebo, L Martelli, Y Su, et al.American Journal of Medical Genetics|December 18, 1996
Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestationsJ B Ravnan, E Chen, M Golabi, et al.Clinical Genetics|July 17, 2001
Rett syndrome from quintuple and triple deletions within the MECP2 deletion hotspot regionR V Lebo, T Ikuta, J M Milunsky, et al.American Journal of Human Genetics|November 1, 1987
Evolutionary implications of the human aldolase-A, -B, -C, and -pseudogene chromosome locationsD R Tolan, J Niclas, B D Bruce, et al.American Journal of Human Genetics|April 1, 1987
The polymorphic locus for glycogen storage disease VI (liver glycogen phosphorylase) maps to chromosome 14C B Newgard, R J Fletterick, L A Anderson, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1986
Human erythropoietin gene: high level expression in stably transfected mammalian cells and chromosome localizationJ S Powell, K L Berkner, R V Lebo, et al.American Journal of Medical Genetics|October 1, 1994
Ancient, highly polymorphic human major histocompatibility complex DQA1 intron sequencesM D McGinnis, R V Lebo, D L Quinn, et al.Journal of Reconstructive Microsurgery|November 14, 1997
DNA amplification determines donor-cell fate in cryopreserved skin allograftsH S Kim, C Meuli-Simmen, H J Buncke, et al.The Journal of Clinical Investigation|June 1, 1979
Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromesS H Embury, R V Lebo, A M Dozy, et al.Pageof 136