Beckwith, J.B.: Extreme cytomegaly of the adrenal fetal cortex, omphalocele, hyperplasia of kidneys and pancreas and Leydig-cell hyperplasia —another syndrome? Presented at the Annual Meeting of Western Society for Pediatric Research, Los Angeles, California, Nov. 11, 1963.
2.
Beckwith, J.B., Wang, C., Donnell, G.N., and Gwinn, J.L.: Hyperplastic fetal visceromegaly with macroglossia, omphalocele, cytomegaly of the adrenal fetal cortex, postnatal somatic gigantism, and other abnormalities: a newly recognized syndrome. Abstract read at Annual Meeting of American Pediatric Society, Seattle, Washington , June 16-18, 1964.
3.
Filippi, G., and McKusick, V.A.: The Beckwith-Wiedemann syndrome; report of two cases and review of literature . Medicine49: 279, 1970.
4.
Bronstein, I.P. , Abelson, S.M., Jeffee, R.H., and Von Bonen , G.: Macroglossia in children; review of literature, report of case of true muscular hypertrophy and suggested classification. Am. J. Dis. Child.54: 1328, 1937 .
5.
Koop, C.E., and Moschakis, E.A.: Capillary lymphangioma of the tongue complicated by glossitis. Pediatrics27: 800, 1961.
6.
Shafer, A.D. : Primary macroglossia. Clin. Pediatr.7: 357, 1968.
7.
Arous, M.S., Solitare, G.B., and Grunt, J.A.: The macroglossia of Beckwith's syndrome. Plast. Reconstr. Surg.45: 341, 1970.
8.
Sherman, F.E. , Bass, L.E., and Fetterman , G.H.: Congenital metastasizing adrenal cortical carcinoma associated with cytomegaly of the fetal adrenal cortex. Am. J. Clin. Pathol.30: 439, 1958.
9.
Neeman, J., cited by Beckwith, J.B. : Macroglossia, omphalocele, adrenal cytomegaly, gigantism and hyperplastic visceromegaly. In Bergsma, D. (Ed.): Birth Defects. Original Article Series 5: 188, 1969.
10.
Wilson, F.C. , and Orlin, H.: Crossed congenital hemihypertrophy associated with Wilm's tumor. J. Bone Joint Surg.47: 1609, 1965 .
11.
Tower, J., and Beck, P.C., cited by Beckwith, J.B. : Macroglossia, omphalocele, adrenal cytomegaly, gigantism and hyperplastic visceromegaly. In Bergsma, D. (Ed.): Birth Defects. Original Article Series 5: 188, 1969.
12.
Beckwith, J.B.: Macroglossia, omphalocele, adrenal cytomegaly, gigantism and hyperplastic visceromegaly. Proceedings of the First Conference on the Clinical Delineation of Birth Defects, Baltimore, Maryland, May 20-25, 1968.
13.
Cohen, M.M. , Gorlin, R.J., Feingold, M., and Bensel, R.W.: The Beckwith-Wiedemann syndrome. Am. J. Dis. Child.122: 515, 1971.
14.
Sotelo-Avila, C., and Singer, D.B.: Syndrome of hyperplastic fetal visceromegaly and neonatal hypoglycemia (Beckwith's Syndrome). Pediatrics46: 240, 1970.
15.
Gellis, S.S. , and Hsia, D.Y.Y.: The infant of the diabetic mother. Am. J. Dis. Child.97: 1, 1959.
16.
Irving, I.: Exomphalos with macroglossia: a study of 11 cases. J Pediatr. Surg.2: 499, 1967.
17.
Ruffie, J., Virenque, J., Bardier, R., and Colombies, P.: Remaniements chromosomiques complexes portant sur les autosomes s'accompaqnant d' anomalies craniofaciales et d'un omphalocele. C. R. Acad. Sci. (Series D) 262: 386, 1966.
18.
Wiedemann, H.R.: Complexe malformatif familial avec hernie ombilicale et macroglossie. Un "syndrome nouveau"? J. Genet. Hum.13: 223, 1964.
19.
Mariani, R. , Unal, D., Spriet, A., Carcassonne, M., and Bernard, R.: Hypoglycemie du nouveau-ne' avec microcephalie macroglossie et megalosplechnie. Arch. Franc. Pediatr.26: 337, 1969.