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Journal Abstract Search

134 related items for PubMed ID: 2018266

  • 1.
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  • 2. Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria.
    Zollino M, Battaglia A, D'Avanzo MG, Della Bruna MM, Marini R, Scarano G, Cappa M, Neri G.
    Am J Med Genet; 1994 Sep 01; 52(3):302-7. PubMed ID: 7810561
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  • 5. Cohen syndrome.
    Alavi S, Kher A, Kumar A, Muranjan M, Bharucha B.
    Indian Pediatr; 1993 May 01; 30(5):678-81. PubMed ID: 8282400
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  • 6. Cerebro-oculo-facio-skeletal (COFS) syndrome. The variability of presenting symptoms as a manifestation of two subtypes?
    Casteels I, Wijnants A, Casaer P, Eggermont E, Misotten L, Fryns JP.
    Genet Couns; 1991 May 01; 2(1):43-6. PubMed ID: 1741976
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  • 8. [Monozygotic twins with Williams-Beuren or 'elfen-face' syndrome].
    Oorthuys JW.
    Tijdschr Kindergeneeskd; 1984 Oct 01; 52(5):197-200. PubMed ID: 6542697
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  • 9. [Cohen syndrome in 2 brothers].
    Zetler S, Römke C, Aksu F.
    Klin Padiatr; 1987 Oct 01; 199(1):55-7. PubMed ID: 3560767
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  • 11. Monozygotic twins discordant for the Russell-Silver syndrome.
    Samn M, Lewis K, Blumberg B.
    Am J Med Genet; 1990 Dec 01; 37(4):543-5. PubMed ID: 2260605
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  • 14. Costello syndrome: the natural history of a true postnatal growth retardation syndrome.
    Umans S, Decock P, Fryns JP.
    Genet Couns; 1995 Dec 01; 6(2):121-5. PubMed ID: 7546454
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  • 15. Identical twins with Cohen syndrome.
    North KN, Fulton AB, Whiteman DA.
    Am J Med Genet; 1995 Jul 31; 58(1):54-8. PubMed ID: 7573157
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  • 16. The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies.
    Herrmann J, Pallister PD, Tiddy W, Opitz JM.
    Birth Defects Orig Artic Ser; 1975 Jul 31; 11(5):7-18. PubMed ID: 1218237
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  • 17. "C" trigonocephaly syndrome with diaphragmnatic hernia.
    Addor MC, Stefanutti D, Farron F, Meinecke P, Lacombe D, Sarlangue J, Prescia G, Schorderet DF.
    Genet Couns; 1995 Jul 31; 6(2):113-20. PubMed ID: 7546453
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  • 18. Lujan-Fryns syndrome (X-linked mental retardation with marfanoid habitus): report of three cases and review.
    Lacombe D, Bonneau D, Verloes A, Couet D, Koulischer L, Battin J.
    Genet Couns; 1993 Jul 31; 4(3):193-8. PubMed ID: 8267926
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  • 19. Fryns syndrome: another example of non-lethal outcome with severe mental handicap.
    Hanssen AM, Schrander-Stumpel CT, Thiry PA, Fryns JP.
    Genet Couns; 1992 Jul 31; 3(4):187-93. PubMed ID: 1472353
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  • 20. Multiple critical smallest region of overlap in monosomy 16Q syndrome?
    Doco-Fenzy M, Elchardus JF, Brami G, Digeon B, Gruson N, Adnet JJ.
    Genet Couns; 1994 Jul 31; 5(1):39-44. PubMed ID: 8031534
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