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Cockayne, E.A. : Dwarfism with retinal atrophy and deafness . Arch. Dis. Child.21: 52, 1946.
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Neill, C.A., and Dingwall, M.D.: A syndrome resembling progeria: Review of two cases. Arch. Dis. Child.25: 213, 1950.
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Marie, J., Leveque, B., and Hesse, J.C.: Nanisme avec retinite pigmentaire (syndrome de Cockayne). Sem. Hop. Paris34: 1101, 1958.
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MacDonald, W.B. , Fitch, K.D., and Lewis, I.C.: Cockayne's syndrome: Heredofamilial disorder of growth and development. Pediatrics25: 997, 1960.
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Uesugi, M., Nakagawa, O., and Uesugi, T.L.: A case regarded as Cockayne's syndrome. Rinsho14: 1777, 1960.
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Cullen, M., and Mora, H.: Cockayne's syndrome. Arch. Agent. Pediatr.55: 16, 1961.
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Spark, H.L.: Cachectic dwarfism resembling the Cockayne-Neill type. J. Pediatr.66: 41, 1965.
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Guzzetta, F. : La sindrome di Cockayne. Min. Pediatr.19: 891, 1967.
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Civantos, F. : Human chromosomal abnormalities. Bull. Tulane Med. Fac.20: 241, 1961.
11.
Windmiller, J., Walley, P.J., and Fink, G.W.: Cockayne syndrome with chromosomal analysis . Am. J. Dis. Child.105: 204, 1963.
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McIntyre, C.A. , Jr., and Brown, H.W.: Twins with cachectic dwarfism. J. Pediatr.67: 1204, 1965.
13.
Paddison, R.M. , Moossy, J., Derbes, V.J., and Kloepfer , W.: Cockayne's syndrome, a report of five new cases with biochemical, chromosomal, dermatologic, genetic and neuropathologic observations. Derm. Trop.2: 195, 1963.
14.
Ohno, T., and Hirooka, M.: Renal lesions in Cockayne's syndrome. Tohoku J. Exp. Med.89: 151, 1966.
15.
Cotton, R.B. , Keats, T.E., and McCoy, E.E.: Abnormal blood glucose regulation in Cockayne's syndrome. Pediatrics46: 54, 1970.
16.
Fujimoto, W.Y. , Greene, M.L., and Seegmiller , J.E.: Cockayne's syndrome, report of a case with hyperinsulinemia, renal disease and normal growth hormone . J. Pediatr.75: 881, 1969.
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Sugarman, G.I. , and Reed, W.B.: Cockayne syndrome: A review and report of two siblings with metabolic studies. XIII Intern. Congress of Pediatr, 111-7C: 319, Sept. 1971.
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Moossy, J.: The neuropathology of Cockayne's syndrome. J. Neuropathol. Exp. Neurol.25: 654, 1967.
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Rowlatt, U. : Cockayne's syndrome. Acta Neuropathol.14: 52, 1969.
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Norman, R.M. , and Tingey, A.H.: Syndrome of micro-encephaly, strio-cerebellar calcifications and leuko-dystrophy. J. Neurol. Neurosurg. Psychiatry29: 157, 1966.
21.
Lyons, G., Robain, O., Philippart, M., and Sarlieve, L.: Leucodystrophie avec calcifications striocerebelleuses, microcephalie et nanisme . Rev. Neurol.119: 197, 1968.
22.
Martin, J.J. , Derberdt, R., Philippart, M., et al.: Peculiar dysorphic syndrome with orthochromatic leucodystrophy. Acta Neuropathol.18: 224, 1971.
23.
Moosa, A., and Dubowitz, V.: Peripheral neuropathy in Cockayne's syndrome. Arch. Dis. Child.45: 674, 1970.
