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PUBMED FOR HANDHELDS

Journal Abstract Search


157 related items for PubMed ID: 3773923

  • 1.
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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]

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  • 5. [EMG syndrome. Review apropo of 2 cases].
    Torres V, Torres CC.
    Med Cutan Ibero Lat Am; 1977 Sep; 5(1):53-8. PubMed ID: 561276
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  • 7. Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family.
    Best LG, Hoekstra RE.
    Am J Med Genet; 1981 Sep; 9(4):291-9. PubMed ID: 7294068
    [Abstract] [Full Text] [Related]

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  • 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]

  • 12.
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  • 13. [The Wiedemann-Beckwith syndrome].
    Bene M.
    Rev Pediatr Obstet Ginecol Pediatr; 1978 Apr 07; 27(1):75-81. PubMed ID: 418483
    [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
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  • 18. [Beckwith Wiedemann syndrom (author's transl)].
    Alain JL, Lassalle JL, Alain J, Moulies D, Terrier G.
    Chir Pediatr; 1978 May 07; 19(4):239-45. PubMed ID: 153802
    [Abstract] [Full Text] [Related]

  • 19. [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]

  • 20. Beckwith-Wiedemann syndrome (exomphalos-macroglossia-gigantism: EMG syndrome).
    Penchaszadeh VB.
    Birth Defects Orig Artic Ser; 1971 Jun 28; 7(7):284-5. PubMed ID: 5173230
    [No Abstract] [Full Text] [Related]


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