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Journal Abstract Search
130 related items for PubMed ID: 424221
1. [[Beckwith-Wiedemann syndrome. Laterospective analysis of omphalocele cases]. Kosztolányi G, Klujber L, Molnár D, Jászai V. Orv Hetil; 1979 Feb 25; 120(8):449-52. PubMed ID: 424221 [No Abstract] [Full Text] [Related]
2. 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 25; 72(5):238-42. PubMed ID: 6932218 [No Abstract] [Full Text] [Related]
3. [Wiedemann-Beckwith syndrome (macroglossia, omphalocele, gigantism)]. Mena M, Strickeler A. Rev Chil Pediatr; 1979 May 25; 50(1):59-61. PubMed ID: 504749 [No Abstract] [Full Text] [Related]
5. [Wiedemann-Beckwith syndrome with hepatoblastoma (author's transl)]. Molina J, Muñoz M, De Miguel C, Martínez-Peñuela JM, Villanueva A, Delgado A. An Esp Pediatr; 1981 Oct 25; 15(4):365-70. PubMed ID: 6279002 [No Abstract] [Full Text] [Related]
6. The Beckwith-Wiedemann syndrome in Nigerian infants (exomphalos, macroglossia and gigantism). Adeyokunnu AA, Adeniyi A. East Afr Med J; 1981 Sep 25; 58(9):684-90. PubMed ID: 7318721 [No Abstract] [Full Text] [Related]
7. [Exaggerated somatomedin activity in the Beckwith-Wiedemann syndrome (author's transl)]. Schabel F, Frisch H. Padiatr Padol; 1979 Sep 25; 14(3):249-57. PubMed ID: 471523 [Abstract] [Full Text] [Related]
8. [Macroglossia in the EMG syndrome]. Schütz P, Ramba J, Zapadlo M. Cesk Stomatol; 1980 Nov 25; 80(6):397-402. PubMed ID: 6934854 [No Abstract] [Full Text] [Related]
9. [EMG syndrome. Review apropo of 2 cases]. Torres V, Torres CC. Med Cutan Ibero Lat Am; 1977 Nov 25; 5(1):53-8. PubMed ID: 561276 [Abstract] [Full Text] [Related]
10. [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]
11. [Wiedemann-Beckwith syndrome. Description of a clinical case with macroglossia, umbilical hernia, hepatonephromegaly, relative microcephaly, macrosomy, and transient hypoglycemia]. Lendvai D, Cardi E, Ballati G, Rezza E. Pediatria (Napoli); 1968 Oct 31; 76(5):738-47. PubMed ID: 5739619 [No Abstract] [Full Text] [Related]
12. [Mediastinal neuroblastoma in Wiedemann-Beckwith syndrome]. Huber A, Gutjahr P. Monatsschr Kinderheilkd; 1989 Apr 31; 137(4):243-4. PubMed ID: 2733702 [Abstract] [Full Text] [Related]
13. 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 Apr 31; 1(1):59-63. PubMed ID: 610426 [Abstract] [Full Text] [Related]
14. Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family. Best LG, Hoekstra RE. Am J Med Genet; 1981 Apr 31; 9(4):291-9. PubMed ID: 7294068 [Abstract] [Full Text] [Related]