RaymondE.TiptonJr.MD

PubMed

• 10 citations
  Ga-67 cardiac uptake.
  Dorothy S. Lin, Raymond E. Tipton> ;Clinical Nuclear Medicine. 1983 Dec 1
• Hohlraum-driven ignitionlike double-shell implosions on the omega laser facility.
  Amendt, P. A., Robey, H. F., Park, H. S., Tipton, R. E., Turner, R. E., Milovich, J. L., Bono, M., Hibbard, R., Louis, H., Wallace, R., Glebov, V. Y.> ;Phys Rev Lett. 2005 Feb 18
• Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 c...
  Pivnick, E. K., Velagaleti, G. V., Wilroy, R. S., Smith, M. E., Rose, S. R., Tipton, R. E., Tharapel, A. T.> ;J Med Genet. 1996 Sep
• Hyperpipecolic acidemia. Occurrence in an infant with clinical findings of the cerebrohepatorenal (Zellweger) syndrome.
  Arneson, D. W., Tipton, R. E., Ward, J. C.> ;Arch Neurol. 1982 Nov
• Growth retardation, alopecia, pseudo-anodontia, and optic atrophy--the GAPO syndrome: report of a patient and review of the literature.
  Tipton, R. E., Gorlin, R. J.> ;Am J Med Genet. 1984 Oct
• Transient leukemoid reaction and trisomy 21 mosaicism in a phenotypically normal newborn.
  Brodeur, G. M., Dahl, G. V., Williams, D. L., Tipton, R. E., Kalwinsky, D. K.> ;Blood. 1980 Apr
• Accelerated skeletal maturation in infancy syndrome: report of a third case.
  Tipton, R. E., Wilroy, R. S., Summitt, R. L.> ;J Pediatr. 1973 Nov 01
• Rapid chromosome analysis with the use of spontaneously dividing cells derived from umbilical cord blood (fetal and neonatal).
  Tipton, R. E., Tharapel, A. T., Chang, H. H., Simpson, J. L., Elias, S.> ;Am J Obstet Gynecol. 1989 Dec
• Diagnosis of trisomy 18 using spontaneously dividing cells from fetal umbilical cord blood: a novel approach for rapid late second and third trimester prenatal diagnosis.
  Tharapel, A. T., Moretti, M. L., Meyers, C. M., Shulman, L. P., Tipton, R. E., Summitt, J. B., Elias, S., Wilroy, R. S., Epps, M., Simpson, J. L.> ;Am J Perinatol. 1990 Jul
• Sialidase (alpha-n-acetyl neuraminidase) deficiency: the enzyme defect in an adult with macular cherry-red spots and myoclonus without dementia.
  Thomas, G. H., Tipton, R. E., Ch'ien, L. T., Reynolds, L. W., Miller, C. S.> ;Clin Genet. 1978 Apr
• Phenotypic heterogeneity in the Noonan syndrome.
  Wilroy, R. S., Summitt, R. L., Tipton, R. E., Primm, P. A., Martens, P. R.> ;Birth Defects Orig Artic Ser. 1979
• Duplication 6q syndrome.
  Tipton, R. E., Berns, J. S., Johnson, W. E., Wilroy, R. S., Summitt, R. L.> ;Am J Med Genet. 1979
• X-autosome translocations: a review.
  Summitt, R. L., Tipton, R. E., Wilroy, R. S., Martens, P. R., Phelan, J. P.> ;Birth Defects Orig Artic Ser. 1978
• The Dubowitz syndrome.
  Wilroy, R. S., Tipton, R. E., Summitt, R. L.> ;Am J Med Genet. 1978
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