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Journal Abstract Search

128 related items for PubMed ID: 6638067

  • 1. 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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  • 6. [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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  • 9. [AREDYLD syndrome].
    Masuno M.
    Ryoikibetsu Shokogun Shirizu; 2001 Feb; (33):218. PubMed ID: 11462408
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  • 11. A previously undescribed ectodermal dysplasia of the tricho-odonto-onychial subgroup in a family.
    Tsakalakos N, Jordaan FH, Taljaard JJ, Hough SF.
    Arch Dermatol; 1986 Sep; 122(9):1047-53. PubMed ID: 3740884
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  • 17. 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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