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79 related items for PubMed ID: 617010
1. [The Beckwith-Wiedemann syndrome]. Banićević M, Joksimović I, Nedeljković V, Papić R, Sićević S. Srp Arh Celok Lek; 1977 Dec; 105(12):1095-1102. PubMed ID: 617010 [No Abstract] [Full Text] [Related]
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 Dec; 1(1):59-63. PubMed ID: 610426 [Abstract] [Full Text] [Related]
3. [Mediastinal neuroblastoma in Wiedemann-Beckwith syndrome]. Huber A, Gutjahr P. Monatsschr Kinderheilkd; 1989 Apr; 137(4):243-4. PubMed ID: 2733702 [Abstract] [Full Text] [Related]
4. The Beckwith-Wiedemann syndrome in Nigerian infants (exomphalos, macroglossia and gigantism). Adeyokunnu AA, Adeniyi A. East Afr Med J; 1981 Sep; 58(9):684-90. PubMed ID: 7318721 [No Abstract] [Full Text] [Related]
5. [Wiedemann-Beckwith syndrome (omphalocele-macroglossia-gigantism)]. Hooft C, Boedts F, Van Acker K. Ann Pediatr (Paris); 1969 Jan 02; 16(1):49-56. PubMed ID: 5791875 [No Abstract] [Full Text] [Related]
6. [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]
7. [Wiedemann-Beckwith syndrome. Study of an oligosymptomatic form]. Lemke J, Meinecke P, Frank HD. Monatsschr Kinderheilkd; 1986 Aug 07; 134(8):554-7. PubMed ID: 3773923 [Abstract] [Full Text] [Related]
8. [The Wiedemann-Beckwith syndrome]. Bene M. Rev Pediatr Obstet Ginecol Pediatr; 1978 Aug 07; 27(1):75-81. PubMed ID: 418483 [No Abstract] [Full Text] [Related]
9. [Beckwith-Wiedemann syndrome or EMG syndrome (Exomphalos-macroglossia-gigantism syndrome)]. Lambotte C, Richelle C, Rigo J, Mativa A, Malchair R. Med Hyg (Geneve); 1979 Mar 28; 37(1326):1088-93. PubMed ID: 286875 [No Abstract] [Full Text] [Related]
10. Nephroblastoma and Beckwith-Wiedemann syndrome. Gruner M, Guilhaume A, Montagne JP, Fauré C. Ann Radiol (Paris); 1981 Jan 28; 24(1):39-42. PubMed ID: 6258469 [No Abstract] [Full Text] [Related]
11. [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; 28(3):281-91. PubMed ID: 7463028 [No Abstract] [Full Text] [Related]
12. [The Beckwith-Wiedemann syndrome. Six observations with three familial forms (author's transl)]. Labbe A, Demeocq F, Gaulme J, Masson A, Malpuech G. Ann Pediatr (Paris); 1981 Nov 28; 28(9):665-70. PubMed ID: 7316412 [No Abstract] [Full Text] [Related]
13. [Exaggerated somatomedin activity in the Beckwith-Wiedemann syndrome (author's transl)]. Schabel F, Frisch H. Padiatr Padol; 1979 Nov 28; 14(3):249-57. PubMed ID: 471523 [Abstract] [Full Text] [Related]
14. Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family. Best LG, Hoekstra RE. Am J Med Genet; 1981 Nov 28; 9(4):291-9. PubMed ID: 7294068 [Abstract] [Full Text] [Related]
15. [Somatomedin activity in Wiedemann-Beckwith syndrome]. Weninger M, Lischka A, Pollak A, Vergesslich C, Ogris E, Frisch H. Monatsschr Kinderheilkd; 1984 Dec 28; 132(12):900-3. PubMed ID: 6395007 [Abstract] [Full Text] [Related]
16. [The Wiedemann-Beckwith syndrome and a congenital cataract]. Momtchilova M, Pelosse B, Laroche L, Vazquez MP. J Fr Ophtalmol; 2001 May 28; 24(5):479-81. PubMed ID: 11397983 [Abstract] [Full Text] [Related]
18. Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new cases. Journel H, Lucas J, Allaire C, Le Mée F, Defawe G, Lecornu M, Jouan H, Roussey M, Le Marec B. Ann Genet; 1985 May 28; 28(2):97-101. PubMed ID: 3876070 [Abstract] [Full Text] [Related]
20. Beckwith-Wiedemann Syndrome (BWS): a case report and literature review. Ogundiran TO, Aghahowa ME, Brown BJ, Irabor DO. West Afr J Med; 2003 May 28; 22(1):101-2. PubMed ID: 12769320 [Abstract] [Full Text] [Related] Page: [Next] [New Search]