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Journal Abstract Search

143 related items for PubMed ID: 6641002

  • 1. Greig cephalopolysyndactyly: report of 13 affected individuals in three families.
    Baraitser M, Winter RM, Brett EM.
    Clin Genet; 1983 Oct; 24(4):257-65. PubMed ID: 6641002
    [Abstract] [Full Text] [Related]

  • 2. The Greig cephalopolysyndactyly syndrome in a Canadian family.
    Chudley AE, Houston CS.
    Am J Med Genet; 1982 Nov; 13(3):269-76. PubMed ID: 6295159
    [No Abstract] [Full Text] [Related]

  • 3. Acrocallosal syndrome: a case report.
    Bonatz E, Descartes M, Tamarapalli JR.
    J Hand Surg Am; 1997 May; 22(3):492-4. PubMed ID: 9195460
    [Abstract] [Full Text] [Related]

  • 4. Two Indian families with Greig cephalopolysyndactyly with non-syndromic phenotype.
    Sethi SK, Goyal D, Khalil S, Yadav DK.
    Eur J Pediatr; 2013 Aug; 172(8):1131-5. PubMed ID: 23334564
    [Abstract] [Full Text] [Related]

  • 5. Variable expressivity of hypertelorism in three siblings with Greig syndrome.
    Gencik A, Genciková A.
    Acta Paediatr Hung; 1986 Aug; 27(2):133-40. PubMed ID: 3756012
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  • 6. A family with one child with acrocallosal syndrome, one child with anencephaly-polydactyly, and parental consanguinity.
    Cataltepe S, Tuncbilek E.
    Eur J Pediatr; 1992 Apr; 151(4):288-90. PubMed ID: 1499582
    [Abstract] [Full Text] [Related]

  • 7. [Hereditary type E brachydactylia. Apropos of a familial case].
    Gnamey D, Walbaum R, Fossati P, Prouvost JM.
    Pediatrie; 1975 Mar; 30(2):153-9. PubMed ID: 165459
    [No Abstract] [Full Text] [Related]

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  • 9. The acrocallosal syndrome in a Turkish boy.
    Yüksel M, Caliskan M, Oğur G, Ozmen M, Dolunay G, Apak S.
    J Med Genet; 1990 Jan; 27(1):48-9. PubMed ID: 2308155
    [Abstract] [Full Text] [Related]

  • 10. Brachydactyly with absence of middle phalanges and hypoplastic nails. A new hereditary syndrome.
    Cuevas-Sosa A, García-Segur F.
    J Bone Joint Surg Br; 1971 Feb; 53(1):101-5. PubMed ID: 4325377
    [No Abstract] [Full Text] [Related]

  • 11. Schinzel acrocallosal syndrome: a variant example of the Greig syndrome?
    Legius E, Fryns JP, Casaer P, Boel M, Eggermont E.
    Ann Genet; 1985 Feb; 28(4):239-40. PubMed ID: 3879437
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  • 13. The Coffin-Lowry syndrome: an inherited faciodigital mental retardation syndrome.
    Temtamy SA, Miller JD, Hussels-Maumenee I.
    J Pediatr; 1975 May; 86(5):724-31. PubMed ID: 1133653
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  • 15. The acrocallosal syndrome and Greig syndrome are not allelic disorders.
    Brueton LA, Chotai KA, van Herwerden L, Schinzel A, Winter RM.
    J Med Genet; 1992 Sep; 29(9):635-7. PubMed ID: 1404293
    [Abstract] [Full Text] [Related]

  • 16. Greig cephalopolysyndactyly syndrome.
    Duncan PA, Klein RM, Wilmot PL, Shapiro LR.
    Am J Dis Child; 1979 Aug; 133(8):818-21. PubMed ID: 223435
    [Abstract] [Full Text] [Related]

  • 17. [Faciodigitogenital syndrome (Aarskog's syndrome)].
    Schrander-Stumpel CT, van Benthem LH, Bijlsma JB.
    Ned Tijdschr Geneeskd; 1985 Apr 13; 129(15):684-8. PubMed ID: 3990863
    [No Abstract] [Full Text] [Related]

  • 18. Tricho-rhino-phalangeal syndrome.
    Kozlowski K, Blaim A, Malolepszy E.
    Australas Radiol; 1972 Dec 13; 16(4):411-6. PubMed ID: 4661984
    [No Abstract] [Full Text] [Related]

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