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Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature

• Barlow GB (1980) Excretion of polyamines by children with Beckwith's syndrome. Arch Dis Child 55:40–42

  Google Scholar 

• Beckwith JB (1969) Macroglossia, omphalocele, adrenal cytomegaly, gigantism and hyperplastic visceromegaly. Birth Defects 5:188–196

  Google Scholar 

• Ben-Galim E, Gross-Kieselstein E, Abrahamov A (1977) Beckwith-Wiedemann syndrome in a mother and her son. Am J Dis Child 131:801–803

  Google Scholar 

• Benke, PJ (1978) Familial Beckwith-Wiedemann syndrome. Birth Defects Conference, San Francisco

  Google Scholar 

• Berry AC, Belton EM, Chanler C (1980) Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counseling. J Med Genet 17:136–138

  Google Scholar 

• Best LG, Hoekstra RE (1980) Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family. Am J Med Genet 9:291–299

  Google Scholar 

• Brissenden JE, Ullrich, A, Francke U (1984) Chromosomal mapping of loci for insulin-like growth factors I and II and for epidermal growth factor in man. Am J Hum Genet 36:133S

  Google Scholar 

• Chemke J (1976) Familial macroglossia-omphalocele syndrome. J Genet Hum 24:271–279

  Google Scholar 

• Cohen MM (1969) Comment on the macroglossia-omphalocele syndrome. Birth Defects 5:197

  Google Scholar 

• Cohen MM, Gorlin RJ, Feingold M, ten Bensel RW (1971) The Beckwith-Wiedemann syndrome. Am J Dis Child 122:515–519

  Google Scholar 

• de Martinville B, Francke U (1983) The c-Ha-ras-1, insulin and B-globin loci map outside the deletion associated with aniridia-Wilms' tumour. Nature 305:641–643

  Google Scholar 

• Eaton AP, Maurer WF (1971) The Beckwith-Wiedemann syndrome. Am J Dis Child 122:520–525

  Google Scholar 

• Eccles MR, Millow LJ, Wilkins RJ, Reeve AE (1984) Harvey-ras allele deletion detected by in situ hybridization to Wilms' tumor chromosomes. Hum Genet 67:190–192

  Google Scholar 

• Emery LG, Shields M, Shah NR, Garbes A (1983) Neuroblastoma associated with Beckwith-Wiedemann syndrome. Cancer 52:176–179

  Google Scholar 

• Filippi G, McKusick VA (1970) The Beckwith-Wiedemann syndrome. Medicine 49:279–298

  Google Scholar 

• Forrester RM (1973) Wiedemann-Beckwith syndrome. Lancet II:47

  Google Scholar 

• Grace JB, Herrman WM, Kornblut AD (1977) Macroglossia in the Beckwith-Wiedemann syndrome. Trans Pa Acad Ophthalmol Otolaryngol 84:116–119

  Google Scholar 

• Greenberg F, Stein F, Gresik MV, Finegold MJ, Carpenter RJ, Riccardi VM, Beaudet AL (1986) The Perlman familial nephroblastomatosis syndrome. Am J Med Genet 24:101–110

  Google Scholar 

• Greene RJ, Gilbert EF, Huang SW, Horowitz S, Levy RL, Herrmann JRP, Hong R (1973) Immunodeficiency associated with exomphalos-macroglossia-gigantism syndrome. J Pediatr 82:814–820

  Google Scholar 

• Greenwood RD, Sommer A, Rosenthal A, Craenen J, Nadas AS (1977) Cardiovascular abnormalities in the Beckwith-Wiedemann syndrome. Am J Dis Child 131:293–294

  Google Scholar 

• Grunt JA, Enriquez AR (1972) Further studies of the hypoglycemia in children with the exomphalos-macroglossia-gigantism syndrome. Yale J Biol Med 45:15–21

  Google Scholar 

• Hadro T, Kleck KA, Khanna N, Pardo J (1985) Wiedemann-Beckwith syndrome: evidence for ovum-medicated autosomal dominant inheritance. Am J Hum Genet 37:A56

  Google Scholar 

• Hamill PVV, Drize TA, Johnson CL, Reed RB, Roche AF, Moore WH (1979) Physical growth: National Center for Health Statistics percentiles. Am. J Clin Nutr 32:607–629

  Google Scholar 

• Hasstedt SJ, Cartwright PE (1979) PAP — Pedigree analysis package. Technical report no. 13. Department of Medical Biophysics and Computing, University of Utah Medical Center

• Healy NP, Hatcher NH, Willey AM (1984) Differential diagnosis of Beckwith-Wiedemann syndrome and duplication 8q. Am J Hum Genet 36:95S

  Google Scholar 

• Ichiba Y, Gardner LI (1975) Metabolic and genetic syndromes of overgrowth. In: Gardner LI (ed) Endocrine and genetic diseases of childhood and adolescence, 2nd edn. Saunders, Philadelphia, pp 1314

  Google Scholar 

• Ikeuchi T (1984) Inhibitory effect of ethidium bromide on mitotic chromosome condensation and its application to high-resolution banding. Cytogenet Cell Genet 38:56–61

  Google Scholar 

• Irving IM (1967) Exomphalos with macroglossia: a study of eleven cases. J Pediatr Surg 2:499–507

  Google Scholar 

• Irving IM (1970) The EMG syndrome (exomphalos, macroglossia, gigantism). Prog Pediatr Surg 1:1–61

  Google Scholar 

• Jeanpierre M, Henry I, Turleau C, Ullrich A, de Grouchy J, Junien C (1985) Beckwith-Wiedemann syndrome (BWS) and 11p15 markers. 8th International Human Gene Mapping Workshop, Helsinki (abstr 173). Cytogenet Cell Genet 40

• Kosseff AL, Herrmann J, Optiz J (1972) The Wiedemann-Beckwith syndrome: genetic considerations and a diagnostic sign. Lancet I:844

  Google Scholar 

• Kosseff AL, Herrmann J, Gilbert EF, Viseskul C, Lubinsky M, Opitz JM (1976) Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Eur J Pediatr 123:139–166

  Google Scholar 

• Lebo RV, Cheung M, Bruce BD, Riccardi VM, Kao F, Kan YW (1985) Mapping parathyroid hormone, B-globin, insulin, and LDH-A genes within the human chromosome 11 short arm by spot blotting sorted chromosomes. Hum Genet 69:316–320

  Google Scholar 

• Lee FA (1972) Radiology of the Beckwith-Wiedemann syndrome. Radiol Clin North Am 10:261–276

  Google Scholar 

• Lubinsky M, Herrmann J, Kosseff AL, Opitz JM (1974) Autosomaldominant sex-dependent transmission of the Wiedemann-Beck-with syndrome. Lancet I:932

  Google Scholar 

• Martinez RM, Ocampo-Campos R, Perez-Arraya R, Coroma-Rivera E, Cantu JM (1985) The Wiedemann-Beckwith syndrome in four sibs including one with associated congenital hypothyroidism. Eur J Pediatr 143:233–235

  Google Scholar 

• Matsuura N, Endo M, Okayasu T, Okuno A (1975) Wiedemann-Beckwith syndrome. Lancet II:508

  Google Scholar 

• Mittra I (1984) Somatomedins and proteolytic bioactivation of prolactin and growth hormone. Cell 38:347–348

  Google Scholar 

• Moncrieff MW, Goldsmith AR, Mann JR, Chance GW (1970) Macroglossia, abnormal umbilicus and hypoglycaemia (Beck-with's syndrome). Postgrad Med J 46:162–166

  Google Scholar 

• Niikawa N, Ishikiriyama S, Takahashi S, Inagawa A, Tonoki H, Ohta Y, Hase N, Kamei T, Kajii T (1986) The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity. Am J Med Genet 24:41–55

  Google Scholar 

• Olney AH, Buehler BA, Waziri M (1985) Beckwith-Wiedemann syndrome in discordant monozygotic twins. David W Smith Workshop on malformations and morphogenesis, Sante Fe

• Perlman M, Goldberg GM, Bar-Ziv J, Danovitch G (1973) Renal hamartomas and nephroblastomatosis with fetal gigantism: a familial syndrome. J Pediatr 83:414–418

  Google Scholar 

• Piussan C, Risbourg B, Lenaerts C, Delvallez N, Gontier MF, Vitse M (1980) Syndrome de Wiedemann et Beckwith. J Genet Hum 28:281–291

  Google Scholar 

• Pueschel SM, Padre-Mendoza T (1984) Chromosome 11 and Beckwith-Wiedemann syndrome. J Pediatr 104:484–485

  Google Scholar 

• Punnett HH, Kistermacher ML, Greene AE, Coriell LL (1974) An (X;1) translocation, balanced, 46 chromosomes. Cytogenet Cell Genet 13:406–407

  Google Scholar 

• Reddy JK, Schimke N, Chang CHJ, Svoboda DJ, Slaven J, Therou L (1972) Beckwith-Wiedemann syndrome. Arch Pathol 94:523–532

  Google Scholar 

• Reeve AE, Housiaux PJ, Gardner RJM, Chewings WE, Grindley RM, Millow LJ (1984) Loss of a Harvey ras allele in sporadic Wilms' tumour. Nature 309:174–176

  Google Scholar 

• Ruffie J, Virenque J, Gardier A, Colombies P (1966) Temaniements chromosomiques complexes portant sur les autosomes s'accompagnant d'un omphalocele. CR Acad Sci Paris 262:386–387

  Google Scholar 

• Saal H, Adler D, Disteche C (1984) High resolution cytogenetics and molecular hybridization studies of the Beckwith-Wiedemann syndrome. Am J Hum Genet 36:110S

  Google Scholar 

• Schiff D, Colle E, Wells D, Stern L (1973) Metabolic aspects of the Beckwith-Wiedemann syndrome. J Pediatr 82:258–262

  Google Scholar 

• Schinzel A (1984) Catalogue of unbalanced chromosome aberrations in man. de Gruyter, New York Berlin

  Google Scholar 

• Shapiro LR, Duncan PA, Davidian MM, Singer N (1982) The placenta in familial Beckwith-Wiedemann syndrome. Birth Defects 18:203–206

  Google Scholar 

• Smith DW (1982) Recognizable patterns of human malformations. Saunders, Philadelphia, pp 130–132

  Google Scholar 

• Sommer A, Cutler EA, Cohen BL, Harper D, Backes C (1977) Familial occurrence of the Wiedemann-Beckwith syndrome and persistent fontanel. Am J Med Genet 1:59–63

  Google Scholar 

• Sotelo-Avila C, Singer DB (1970) Syndrome of hyperplastic fetal visceromegaly and neonatal hypoglycemia (Beckwith's syndrome). Pediatrics 46:240–251

  Google Scholar 

• Sotelo-Avila C, Gonzalez-Crussi F, Fowler JW (1980) Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential. J Pediatr 96:47–50

  Google Scholar 

• Spencer GSG, Schabel F, Frisch H (1980) Raised somatomedin associated with normal growth hormone (a cause of Beckwith-Wiedemann syndrome?). Arch Dis Child 55:151–153

  Google Scholar 

• SPSS Inc (1983) SPSS users guide. McGraw-Hill, New York

  Google Scholar 

• Thorburn MJ, Miller CG, Smith-Read EH (1970) Exomphalosmacroglossia-gigantism syndrome in Jamaican infants. Am J Dis Child 119:316–321

  Google Scholar 

• Turleau C, de Grouchy J (1985) Beckwith-Wiedemann syndrome with and without trisomy 11p15. Clin Genet 27:343

  Google Scholar 

• Turleau C, de Grouchy J, Chavin-Colin F, Martelli H, Voyer M, Charlas R (1984) Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases. Hum Genet 67:219–221

  Google Scholar 

• Waziri M, Patil SR, Hanson JW, Bartley JA (1983) Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome. J Pediatr 102:873–876

  Google Scholar 

• Weinstein L, Anderson C (1980) In utero diagnosis of Beckwith-Wiedemann syndrome by ultrasound. Radiology 134:474

  Google Scholar 

• Wiedemann HR (1964) Complexe malformatif familial avec hernie ombilicale et macroglossie — un syndrome nouveau? J Genet Hum 13:223–232

  Google Scholar 

• Wiedemann HR (1983) Tumours and hemihypertrophy associated with Wiedemann-Beckwith syndrome. Eur J Pediatr 141:129

  Google Scholar 

• Winter SC, Curry CJR, Smith JC, Kassel S, Miller L, Andrea J (1986) Prenatal diagnosis of the Beckwith-Wiedemann syndrome. Am J Med Genet 24:137–141

  Google Scholar 

• Wojciechowski AH, Pritchard J (1981) Beckwith-Wiedemann (exomphalos-macroglossia-gigantism-EMG) syndrome and malignant lymphoma. Eur J Pediatr 137:317–321

  Google Scholar 

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