Publications by authors named "RE Tipton"

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D
Demonstration of a Novel Radiochemical Mix Diagnostic for Fusion Implosions at the National Ignition Facility.
S A MacLaren, E L Dewald, D A Martinez, N Gharibyan, K Moody, R E Tipton

Phys Rev Lett· August 2025

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Achievement of Target Gain Larger than Unity in an Inertial Fusion Experiment.
H Abu-Shawareb, R Acree, P Adams, J Adams, B Addis, R E Tipton

Phys Rev Lett· February 2024

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Lawson Criterion for Ignition Exceeded in an Inertial Fusion Experiment.
H Abu-Shawareb, R Acree, P Adams, J Adams, B Addis, R E Tipton

Phys Rev Lett· August 2022

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Measurements of an ablator-gas atomic mix in indirectly driven implosions at the National Ignition Facility.
V A Smalyuk, R E Tipton, J E Pino, D T Casey, G P Grim

Phys Rev Lett· January 2014

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Measurement of the T + T neutron spectrum using the national ignition facility.
D B Sayre, C R Brune, J A Caggiano, V Y Glebov, R Hatarik, R E Tipton

Phys Rev Lett· August 2013

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Hohlraum-driven ignitionlike double-shell implosions on the omega laser facility.
Peter A Amendt, Harry F Robey, H-S Park, R E Tipton, R E Turner

Phys Rev Lett· February 2005

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Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.
E K Pivnick, G V Velagaleti, R S Wilroy, M E Smith, S R Rose, R E Tipton

J Med Genet· September 1996

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Three-dimensional single mode Rayleigh-Taylor experiments on nova.
MM Marinak, BA Remington, SV Weber, RE Tipton, SW Haan

Phys Rev Lett· November 1995

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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.
A T Tharapel, M L Moretti, C M Meyers, L P Shulman, R E Tipton

Am J Perinatol· July 1990

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Rapid chromosome analysis with the use of spontaneously dividing cells derived from umbilical cord blood (fetal and neonatal).
R E Tipton, A T Tharapel, H H Chang, J L Simpson, S Elias

Am J Obstet Gynecol· December 1989

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Growth retardation, alopecia, pseudo-anodontia, and optic atrophy--the GAPO syndrome: report of a patient and review of the literature.
R E Tipton, R J Gorlin

Am J Med Genet· October 1984

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T
The Dubowitz syndrome.
R S Wilroy, R E Tipton, R L Summitt

Am J Med Genet· January 1984

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G
Ga-67 cardiac uptake.
D S Lin, R E Tipton

Clin Nucl Med· December 1983

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H
Hyperpipecolic acidemia. Occurrence in an infant with clinical findings of the cerebrohepatorenal (Zellweger) syndrome.
D W Arneson, R E Tipton, J C Ward

Arch Neurol· November 1982

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Phenotypic heterogeneity in the Noonan syndrome.
R S Wilroy, R L Summitt, R E Tipton, P A Primm, P R Martens

Birth Defects Orig Artic Ser· April 1980

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T
Transient leukemoid reaction and trisomy 21 mosaicism in a phenotypically normal newborn.
G M Brodeur, G V Dahl, D L Williams, R E Tipton, D K Kalwinsky

Blood· April 1980

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D
Duplication 6q syndrome.
R E Tipton, J S Berns, W E Johnson, R S Wilroy, R L Summitt

Am J Med Genet· October 1979

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X
X-autosome translocations: a review.
R L Summitt, R E Tipton, R S Wilroy, P R Martens, J P Phelan

Birth Defects Orig Artic Ser· March 1979

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S
Sialidase (alpha-n-acetyl neuraminidase) deficiency: the enzyme defect in an adult with macular cherry-red spots and myoclonus without dementia.
G H Thomas, R E Tipton, L T Ch'ien, L W Reynolds, C S Miller

Clin Genet· April 1978

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A
Accelerated skeletal maturation in infancy syndrome: report of a third case.
R E Tipton, R S Wilroy, R L Summitt

J Pediatr· November 1973

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Leber's congenital amaurosis and mental retardation.
R E Tipton, I E Hussels

Birth Defects Orig Artic Ser· March 1971

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Myotonic dystrophy with mental retardation.
R E Tipton

Birth Defects Orig Artic Ser· February 1971

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Familial hydrocephalus.
R E Tipton

Birth Defects Orig Artic Ser· February 1971

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Three unusual trisomic patterns in children. Triple X plus triple E-triple X mosaic: normal XY-D trisomy mosaic; partial trisomy with E translocation.
E Engel, J E Haddow, J F Lewis, R E Tipton, J C Overall

Am J Dis Child· March 1967

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PH1-positive chronic myelogenous leukemia, with absence of another G chromosome, in a male.
E Engel, D E Jenkins, R E Tipton, B J McGee, M Engel-de Montmollin

N Engl J Med· September 1965

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