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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

248 related items for PubMed ID: 9555582

  • 1. Congenital camptodactyly associated with the 48,XXYY syndrome.
    Bosch AM, Hack WW, Schrander-Stumpel CT.
    Genet Couns; 1998; 9(1):19-21. PubMed ID: 9555582
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  • 3. [Congenital windblown hand position of the fingers].
    Grünert J, Brug E.
    Z Orthop Ihre Grenzgeb; 1991; 129(5):426-30. PubMed ID: 1836698
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  • 5. The 48,XXYY syndrome.
    Sørensen K, Nielsen J, Jacobsen P, Rølle T.
    J Ment Defic Res; 1978 Sep; 22(3):197-205. PubMed ID: 568179
    [No Abstract] [Full Text] [Related]

  • 6. Analysing human developmental abnormalities.
    Winter RM.
    Bioessays; 1996 Dec; 18(12):965-71. PubMed ID: 8976153
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  • 8. Cytogenetics of müllerian agenesis. A case report.
    Jaffe SB, Loucopoulos A, Jewelewicz R.
    J Reprod Med; 1992 Mar; 37(3):242-6. PubMed ID: 1564711
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  • 10. Symbrachydactyly involving hands and feet.
    De Smet L, Fabry G, Fryns JP.
    Genet Couns; 1998 Mar; 9(1):23-7. PubMed ID: 9555583
    [Abstract] [Full Text] [Related]

  • 11. Double trisomy 48,XXX,+ 18 in a newborn.
    Rosenfeld W, Verma RS, Jhaveri RC, Salazar D, Dosik H.
    Am J Med Genet; 1981 Mar; 8(1):67-71. PubMed ID: 7246607
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  • 14. Catel-Manzke syndrome: two new patients and a critical review of the literature.
    Manzke H, Lehmann K, Klopocki E, Caliebe A.
    Eur J Med Genet; 2008 Mar; 51(5):452-65. PubMed ID: 18501694
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  • 16. The acrofacial dysostoses--a wide spectrum of overlapping phenotypes.
    Dimitrov B, Balikova I, Bradinova I, Zahariev D, Popova A, Simeonov E, De Smet L, Devriendt K, Fryns JP.
    Genet Couns; 2005 Mar; 16(2):181-6. PubMed ID: 16080300
    [No Abstract] [Full Text] [Related]

  • 17. XXXXY syndrome: report of case.
    Boraz RA.
    J Clin Pediatr Dent; 1995 Mar; 19(2):143-6. PubMed ID: 7577735
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  • 19. 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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  • 20. An XXYY male with schizophrenia.
    Lee JW.
    Aust N Z J Psychiatry; 1996 Aug 15; 30(4):553-6. PubMed ID: 8887709
    [Abstract] [Full Text] [Related]

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