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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

247 related items for PubMed ID: 1633641

  • 1. Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?
    van Maldergem L, Wetzburger C, Verloes A, Fourneau C, Gillerot Y.
    Clin Genet; 1992 Jan; 41(1):22-4. PubMed ID: 1633641
    [Abstract] [Full Text] [Related]

  • 2. Cerebro-facio-articular syndrome of Van Maldergem: confirmation of a new MR/MCA syndrome.
    Zampino G, Colosimo C, Balducci F, Mariotti P, Serra F, Scarano G, Mastroiacovo P.
    Clin Genet; 1994 Mar; 45(3):140-4. PubMed ID: 8026105
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  • 3. A three generations family with blepharo-naso-facial malformations suggestive of Pashayan syndrome.
    Stoll C, Terzic J, Fischbach M.
    Genet Couns; 1999 Mar; 10(4):337-43. PubMed ID: 10631920
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  • 5. Inguinal hernia and atrial septal defect in Tel Hashomer camptodactyly syndrome: report of a new case expanding the phenotypic spectrum of the disease.
    Franceschini P, Vardeu MP, Signorile F, Testa A, Guala A, Franceschini D, Dalforno L.
    Am J Med Genet; 1993 May 15; 46(3):341-4. PubMed ID: 8488882
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  • 6. Hunter-McAlpine syndrome: report of a third family.
    Adès LC, Morris LL, Simpson DA, Haan EA.
    Clin Dysmorphol; 1993 Apr 15; 2(2):123-30. PubMed ID: 8281273
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  • 8. A second family with blepharo-naso-facial syndrome.
    Allanson JE.
    Clin Dysmorphol; 2002 Jul 15; 11(3):191-4. PubMed ID: 12072799
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  • 12. [A dominant syndrome associated with polysyndactyly, spatule thumb, facial abnormalities, and mental retardation. (A particular form of Noack's acrocephalosyndactylia)].
    Gnamey D, Farriaux JP.
    J Genet Hum; 1971 Dec 15; 19(4):299-316. PubMed ID: 5152131
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  • 13. Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?
    Filippi G.
    Am J Med Genet; 1985 Dec 15; 22(4):821-4. PubMed ID: 4073130
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  • 15. Rubinstein-Taybi syndrome.
    Berry AC.
    J Med Genet; 1987 Sep 15; 24(9):562-6. PubMed ID: 3312608
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  • 17. An apparently new mental retardation syndrome in three elderly sisters.
    Viljoen DL, Kallis J, Voges S, Marais AS, van Vuuren I.
    Clin Genet; 1991 Jul 15; 40(1):6-11. PubMed ID: 1884519
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  • 19. Coffin-Siris syndrome with multiple congenital malformations and intrauterine death: towards a better delineation of the severe end of the spectrum.
    Coulibaly B, Sigaudy S, Girard N, Popovici C, Missirian C, Heckenroth H, Tasei AM, Fernandez C.
    Eur J Med Genet; 2010 Jul 15; 53(5):318-21. PubMed ID: 20624500
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  • 20. Mutations in TGDS associated with additional malformations of the middle fingers and halluces: Atypical Catel-Manzke syndrome in a fetus.
    Schoner K, Bald R, Horn D, Rehder H, Kornak U, Ehmke N.
    Am J Med Genet A; 2017 Jun 15; 173(6):1694-1697. PubMed ID: 28422407
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