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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

200 related items for PubMed ID: 1345512

  • 1. Ectrodactyly-mandibulo-facial dysostosis: case report and delineation of an entity.
    Turnpenny PD, Johnston AW, Dean JC, Haites NE, Couzin DA, Stephen GS.
    Clin Dysmorphol; 1992 Apr; 1(2):103-9. PubMed ID: 1345512
    [Abstract] [Full Text] [Related]

  • 2. Postaxial acrofacial dysostosis: report of a Brazilian patient.
    Richieri-Costa A, Guion-Almeida ML.
    Am J Med Genet; 1989 Aug; 33(4):447-9. PubMed ID: 2596501
    [Abstract] [Full Text] [Related]

  • 3. Ectrodactyly (split-hand/split-foot) and ectodermal dysplasia with normal lip and palate in a four-generation kindred.
    Wallis CE.
    Clin Genet; 1988 Oct; 34(4):252-7. PubMed ID: 3233778
    [Abstract] [Full Text] [Related]

  • 4. Autosomal dominant inheritance of tetramelic monodactyly.
    Sommer A, Hines SJ.
    Am J Med Genet; 1992 Jan 01; 42(1):51-4. PubMed ID: 1308366
    [Abstract] [Full Text] [Related]

  • 5. Atypical postaxial acrofacial dysostosis (AFD): diabetic embryopathy or a new AFD syndrome?
    Richieri-Costa A, Guion-Almeida ML.
    Am J Med Genet; 1989 Aug 01; 33(4):450-2. PubMed ID: 2596502
    [Abstract] [Full Text] [Related]

  • 6. Ectrodactyly of hands and feet in a child with a complex translocation including 7q21.2.
    Sharland M, Patton MA, Hill L.
    Am J Med Genet; 1991 Jun 15; 39(4):413-4. PubMed ID: 1877619
    [Abstract] [Full Text] [Related]

  • 7. RSH (Smith-Lemli-Opitz) syndrome: "severe" phenotype with ectrodactyly.
    de Jong G, Kirby PA, Muller LM.
    Am J Med Genet; 1998 Jan 23; 75(3):283-7. PubMed ID: 9475598
    [Abstract] [Full Text] [Related]

  • 8. [Familial case of the syndrome of ectrodactyly and mandibulo-facial dysostosis].
    Fontaine G, Farriaux JP, Delattre P, Gidlecki Z, Poupard B, Durieux G, Piquet JJ.
    J Genet Hum; 1974 Dec 23; 22(4):289-307. PubMed ID: 4376815
    [No Abstract] [Full Text] [Related]

  • 9. Bilateral complete radioulnar synostosis associated with ectrodactyly and sensorineural hearing loss: a variant of SHFM1.
    Debeer P, Vandenbossche L, de Ravel TJ, Desloovere C, De Smet L, Huysmans C, Thoelen R, Vermeesch J, Van de Ven WJ, Fryns JP.
    Clin Genet; 2004 Feb 23; 65(2):153-5. PubMed ID: 14984476
    [No Abstract] [Full Text] [Related]

  • 10. Congenital cleft foot and hand.
    Sharma S, Chhetri A, Singh A.
    Indian Pediatr; 1999 Sep 23; 36(9):935-8. PubMed ID: 10744877
    [No Abstract] [Full Text] [Related]

  • 11. [An extensive form of mandibulo-facial dysostosis].
    Genée E.
    J Genet Hum; 1969 May 23; 17(1):45-52. PubMed ID: 5808539
    [No Abstract] [Full Text] [Related]

  • 12. Acrofacial dysostosis of unknown type: nosology of the acrofacial dysostoses.
    Preis S, Raymaekers-Buntinx I, Majewski F.
    Am J Med Genet; 1995 Mar 27; 56(2):155-60. PubMed ID: 7625437
    [Abstract] [Full Text] [Related]

  • 13. EEC syndrome without ectrodactyly: report of two new families.
    Fryns JP, Legius E, Dereymaeker AM, Van den Berghe H.
    J Med Genet; 1990 Mar 27; 27(3):165-8. PubMed ID: 2325090
    [Abstract] [Full Text] [Related]

  • 14. Acrodysostosis: autosomal dominant transmission.
    Sheela SR, Perti A, Thomas G.
    Indian Pediatr; 2005 Aug 27; 42(8):822-6. PubMed ID: 16141486
    [Abstract] [Full Text] [Related]

  • 15. Ectrodactyly and proximal/intermediate interstitial deletion 7q.
    McElveen C, Carvajal MV, Moscatello D, Towner J, Lacassie Y.
    Am J Med Genet; 1995 Mar 13; 56(1):1-5. PubMed ID: 7747769
    [Abstract] [Full Text] [Related]

  • 16. Ectrodactyly, cleft lip/palate syndrome.
    Rodini ES, Freitas JA, Richieri-Costa A.
    Am J Med Genet; 1991 Mar 15; 38(4):539-41. PubMed ID: 2063894
    [Abstract] [Full Text] [Related]

  • 17. Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27.
    van Bokhoven H, Jung M, Smits AP, van Beersum S, Rüschendorf F, van Steensel M, Veenstra M, Tuerlings JH, Mariman EC, Brunner HG, Wienker TF, Reis A, Ropers HH, Hamel BC.
    Am J Hum Genet; 1999 Feb 15; 64(2):538-46. PubMed ID: 9973291
    [Abstract] [Full Text] [Related]

  • 18. Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family.
    Richieri-Costa A, Guion-Almeida ML, Pagnan NA.
    Am J Med Genet; 1992 Dec 01; 44(6):800-2. PubMed ID: 1481850
    [Abstract] [Full Text] [Related]

  • 19. Acrodysostosis in two generations: an autosomal dominant syndrome.
    Hernández RM, Miranda A, Kofman-Alfaro S.
    Clin Genet; 1991 May 01; 39(5):376-82. PubMed ID: 1860254
    [Abstract] [Full Text] [Related]

  • 20. Anonychia and absence/hypoplasia of distal phalanges (Cooks syndrome): report of a second family.
    Nevin NC, Thomas PS, Eedy DJ, Shepherd C.
    J Med Genet; 1995 Aug 01; 32(8):638-41. PubMed ID: 7473658
    [Abstract] [Full Text] [Related]

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