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2. Familial occurrence of the Wiedemann-Beckwith syndrome and persistent fontanel. Sommer A, Cutler EA, Cohen BL, Harper D, Backes C. Am J Med Genet; 1977; 1(1):59-63. PubMed ID: 610426 [Abstract] [Full Text] [Related]
3. [Wiedemann and Beckwith syndrome: a new familial case]. Piussan C, Risbourg B, Lenaerts C, Delvallez N, Gontier MF, Vitse M. J Genet Hum; 1980 Sep; 28(3):281-91. PubMed ID: 7463028 [No Abstract] [Full Text] [Related]
10. [Exomphalos-macroglossia-gigantism syndrome (Wiedemann-Beckwith syndrome) in three siblings]. Bohlmann HG, Havers W. Arch Kinderheilkd; 1971 Jul; 183(2):175-82. PubMed ID: 5567033 [No Abstract] [Full Text] [Related]
11. [Clinical case of the Wiedemann-Beckwith syndrome]. Buttitta P, Pasta G. Minerva Pediatr; 1977 Apr 07; 29(12):855-8. PubMed ID: 875961 [No Abstract] [Full Text] [Related]
14. [Mediastinal neuroblastoma in Wiedemann-Beckwith syndrome]. Huber A, Gutjahr P. Monatsschr Kinderheilkd; 1989 Apr 07; 137(4):243-4. PubMed ID: 2733702 [Abstract] [Full Text] [Related]
15. [Exaggerated somatomedin activity in the Beckwith-Wiedemann syndrome (author's transl)]. Schabel F, Frisch H. Padiatr Padol; 1979 Apr 07; 14(3):249-57. PubMed ID: 471523 [Abstract] [Full Text] [Related]
16. Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling. Berry AC, Belton EM, Chantler C. J Med Genet; 1980 Apr 07; 17(2):136-8. PubMed ID: 7189783 [Abstract] [Full Text] [Related]
17. Two cases of Beckwith-Wiedemann syndrome, one with hemihypertrophy. Bravo Velázquez D, Toro-Solá MA, Muñóz AI, Montes-Jordán V. Bol Asoc Med P R; 1980 May 07; 72(5):238-42. PubMed ID: 6932218 [No Abstract] [Full Text] [Related]