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Journal Abstract Search

199 related items for PubMed ID: 1590979

  • 1. Arthrogryposis, ectodermal dysplasia and other anomalies in two sisters.
    Stoll C, Alembik Y, Finck S, Janser B.
    Genet Couns; 1992; 3(1):35-9. PubMed ID: 1590979
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  • 2. Odontoonychodermal dysplasia: a previously apparently undescribed ectodermal dysplasia.
    Fadhil M, Ghabra TA, Deeb M, Der Kaloustian VM.
    Am J Med Genet; 1983 Feb; 14(2):335-46. PubMed ID: 6837628
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  • 3. Autosomal recessive micrencephaly with simplified gyral pattern, abnormal myelination and arthrogryposis.
    Sztriha L, Al-Gazali LI, Várady E, Goebel HH, Nork M.
    Neuropediatrics; 1999 Jun; 30(3):141-5. PubMed ID: 10480209
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  • 11. Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome-McKusick 10030): further suggestion of autosomal recessive inheritance.
    Sybert VP.
    Am J Med Genet; 1989 Feb; 32(2):266-7. PubMed ID: 2929669
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  • 13. Odontoonychodysplasia with alopecia: a new pure ectodermal dysplasia with probable autosomal recessive inheritance.
    Pinheiro M, Freire-Maia N, Gollop TR.
    Am J Med Genet; 1985 Jan; 20(1):197-202. PubMed ID: 2982262
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  • 14. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E, Palmieri A, Bertola A, Bellini C.
    Genet Couns; 1995 Jan; 6(4):309-12. PubMed ID: 8775417
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  • 15. [Pigmentosum retinis and tubulo-interstitial nephronophtisis in Sensenbrenner syndrome: a case report].
    Costet C, Betis F, Bérard E, Tsimaratos M, Sigaudy S, Antignac C, Gastaud P.
    J Fr Ophtalmol; 2000 Feb; 23(2):158-60. PubMed ID: 10705117
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  • 16. A new autosomal recessive disorder resembling Weaver syndrome.
    Teebi AS, Sundareshan TS, Hammouri MY, al-Awadi SA, al-Saleh QA.
    Am J Med Genet; 1989 Aug; 33(4):479-82. PubMed ID: 2596508
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  • 17. Trichoodontoonychial dysplasia--a new meso-ectodermal dysplasia.
    Pinheiro M, Freire-Maia N, Roth AJ.
    Am J Med Genet; 1983 May; 15(1):67-70. PubMed ID: 6859125
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  • 18. Novel mutations in the EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia.
    Naeem M, Muhammad D, Ahmad W.
    Br J Dermatol; 2005 Jul; 153(1):46-50. PubMed ID: 16029325
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  • 19. Limb pterygium syndromes: a review and report of eleven patients.
    Hall JG, Reed SD, Rosenbaum KN, Gershanik J, Chen H, Wilson KM.
    Am J Med Genet; 1982 Aug; 12(4):377-409. PubMed ID: 7124793
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  • 20. [Hidrotic ectodermal dysplasia].
    Altmeyer P, Schindera I.
    Hautarzt; 1975 Dec; 26(12):631-7. PubMed ID: 1213883
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