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Journal Abstract Search

169 related items for PubMed ID: 7316412

  • 1. [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(9):665-70. PubMed ID: 7316412
    [No Abstract] [Full Text] [Related]

  • 2. [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
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  • 3. 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 Sep; 1(1):59-63. PubMed ID: 610426
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  • 4. [Mediastinal neuroblastoma in Wiedemann-Beckwith syndrome].
    Huber A, Gutjahr P.
    Monatsschr Kinderheilkd; 1989 Apr; 137(4):243-4. PubMed ID: 2733702
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  • 8. [Beckwith Wiedemann syndrom (author's transl)].
    Alain JL, Lassalle JL, Alain J, Moulies D, Terrier G.
    Chir Pediatr; 1978 Apr; 19(4):239-45. PubMed ID: 153802
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  • 12. [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
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  • 16. [Family with Wiedemann-Beckwith syndrome].
    Matsuura N, Okayasu T, Endo M, Anakura M, Okuno A.
    Horumon To Rinsho; 1975 Jun 02; 23(6):626-30. PubMed ID: 1170983
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  • 17. [Hemihypertrophy with wiedemann-Beckwith-syndrome (author's transl)].
    Schenck RD.
    Z Orthop Ihre Grenzgeb; 1976 Jun 02; 114(3):354-60. PubMed ID: 941479
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  • 19. Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling.
    Berry AC, Belton EM, Chantler C.
    J Med Genet; 1980 Apr 02; 17(2):136-8. PubMed ID: 7189783
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  • 20. Exomphalos-macroglossia-gigantism, or EMG syndrome (Beckwith-Wiedemann syndrome).
    Mil Med; 1976 Jul 02; 141(7):467-474. PubMed ID: 819872
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