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Journal Abstract Search

239 related items for PubMed ID: 8042668

  • 41.
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  • 43. AREDYLD: a syndrome combining an acrorenal field defect, ectodermal dysplasia, lipoatrophic diabetes, and other manifestations.
    Pinheiro M, Freire-Maia N, Chautard-Freire-Maia EA, Araujo LM, Liberman B.
    Am J Med Genet; 1983 Sep; 16(1):29-33. PubMed ID: 6638067
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  • 44. [Aplasia of the premolars as a leading symptom of ectodermal dysplasia].
    Weyers H.
    Dtsch Zahnarztl Z; 1980 Aug; 35(8):836-40. PubMed ID: 6935039
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  • 45. [Familial ectodermal dysplasia with agenesis of the breasts and the external urethral sphincter. Description of a case].
    Triolo O, Allegra A, Stella Brienza L, De Meo A, Tropea G.
    Minerva Ginecol; 1993 Mar; 45(3):139-42. PubMed ID: 8332280
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  • 46. Ullrich-Turner syndrome with unilateral agenesis of breast, nipple, and pectoralis major.
    Cohen A, Lavagetto A, Romano C.
    Am J Med Genet; 1992 Sep 01; 44(1):11-2. PubMed ID: 1519640
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  • 49. A case of multiple skeletal anomalies, ectodermal dysplasia, and severe growth and mental retardation.
    Schinzel A.
    Helv Paediatr Acta; 1980 Jul 01; 35(3):243-51. PubMed ID: 6250998
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  • 50. Finlay-Marks (SEN) syndrome: a sporadic case and the delineation of the syndrome.
    Sobreira NL, Brunoni D, Cernach MC, Perez AB.
    Am J Med Genet A; 2006 Feb 01; 140(3):300-2. PubMed ID: 16411189
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  • 51.
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  • 52. Further examples of autosomal dominant transmission of nonsyndromic aplasia cutis congenita.
    Elliott AM, Teebi AS.
    Am J Med Genet; 1997 Dec 31; 73(4):495-6. PubMed ID: 9415483
    [No Abstract] [Full Text] [Related]

  • 53. Another adult with Meier-Gorlin syndrome--insights into the natural history.
    Shalev SA, Hall JG.
    Clin Dysmorphol; 2003 Jul 31; 12(3):167-9. PubMed ID: 14564153
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  • 54.
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  • 55. A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.
    Tariq M, Chishti MS, Ali G, Ahmad W.
    Ann Hum Genet; 2008 Jan 31; 72(Pt 1):19-25. PubMed ID: 18184143
    [Abstract] [Full Text] [Related]

  • 56. Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome?
    Teebi AS, Kaurah P.
    Am J Med Genet; 1996 Dec 18; 66(3):257-60. PubMed ID: 8985482
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  • 57. Bartsocas-Papas syndrome in an Arab family with four affected sibs: further characterization.
    Massoud AA, Ammaari AN, Khan AS, ven Katraman B, Teebi AS.
    Am J Med Genet; 1998 Aug 27; 79(1):16-21. PubMed ID: 9738862
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  • 59. Clinical and molecular analysis of nine families with Adams-Oliver syndrome.
    Verdyck P, Holder-Espinasse M, Hul WV, Wuyts W.
    Eur J Hum Genet; 2003 Jun 27; 11(6):457-63. PubMed ID: 12774039
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  • 60.
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