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Journal Abstract Search

159 related items for PubMed ID: 7304669

  • 21. [Trichothiodystrophy: progresssive manifestations].
    Foulc P, Jumbou O, David A, Sarasin A, Stalder JF.
    Ann Dermatol Venereol; 1999 Oct; 126(10):703-7. PubMed ID: 10604009
    [Abstract] [Full Text] [Related]

  • 22. [Ectodermal dysplasia: multiple manifestations of a hereditary disease].
    Ouellet B, Agha-Amiri M, Dubé-Baril C, Mascrès C.
    J Can Dent Assoc; 1997 May; 63(5):377-81. PubMed ID: 9182019
    [Abstract] [Full Text] [Related]

  • 23. Brief clinical report: new, autosomal dominant form of ectodermal dysplasia.
    Tuffli GA, Laxova R.
    Am J Med Genet; 1983 Feb; 14(2):381-4. PubMed ID: 6837633
    [Abstract] [Full Text] [Related]

  • 24. Family with autosomal dominant hidrotic ectodermal dysplasia: a previously unrecognised syndrome?
    Christianson AL, Fourie S.
    Am J Med Genet; 1996 Jun 28; 63(4):549-53. PubMed ID: 8826433
    [Abstract] [Full Text] [Related]

  • 25. Hereditary anhidrotic ectodermal dysplasia in a Zambian family.
    Sehgal D, Chawla V, Maguire MJ.
    East Afr Med J; 1981 May 28; 58(5):374-9. PubMed ID: 7285838
    [No Abstract] [Full Text] [Related]

  • 26. [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 28; 23(2):158-60. PubMed ID: 10705117
    [Abstract] [Full Text] [Related]

  • 27. Ectodermal dysplasia showing clinical overlap between AEC, Rapp-Hodgkin and CHAND syndromes.
    Sahin MT, Türel-Ermertcan A, Chan I, McGrath JA, Oztürkcan S.
    Clin Exp Dermatol; 2004 Sep 28; 29(5):486-8. PubMed ID: 15347331
    [Abstract] [Full Text] [Related]

  • 28. A previously undescribed condition: tricho-odonto-onycho-dermal syndrome. A review of the tricho-odonto-onychial subgroup of ectodermal dysplasias.
    Pinheiro M, Pereira LC, Freire-Maia N.
    Br J Dermatol; 1981 Oct 28; 105(4):371-82. PubMed ID: 7295550
    [Abstract] [Full Text] [Related]

  • 29. [Hair diseases in children].
    Romanenko GF.
    Vestn Dermatol Venerol; 1980 Apr 28; (4):20-5. PubMed ID: 6249054
    [No Abstract] [Full Text] [Related]

  • 30. Cardio-facio-cutaneous (CFC) syndrome in a child carrying an inherited inversion of chromosome 7.
    Lopez-Rangel E, Hrynchak M, Friedman JM.
    Am J Med Genet; 1993 Sep 01; 47(3):326-9. PubMed ID: 8135275
    [Abstract] [Full Text] [Related]

  • 31. Oculodentodigital dysplasia: study of ophthalmological and clinical manifestations in three boys with probably autosomal recessive inheritance.
    Frasson M, Calixto N, Cronemberger S, de Aguiar RA, Leão LL, de Aguiar MJ.
    Ophthalmic Genet; 2004 Sep 01; 25(3):227-36. PubMed ID: 15512999
    [Abstract] [Full Text] [Related]

  • 32. Autosomal dominant ectodermal dysplasia with significant dental defects.
    Redpath TH, Winter GB.
    Br Dent J; 1969 Feb 04; 126(3):123-8. PubMed ID: 5254120
    [No Abstract] [Full Text] [Related]

  • 33. Odontoonychodermal dysplasia: a previously apparently undescribed ectodermal dysplasia.
    Fadhil M, Ghabra TA, Deeb M, Der Kaloustian VM.
    Am J Med Genet; 1983 Feb 04; 14(2):335-46. PubMed ID: 6837628
    [Abstract] [Full Text] [Related]

  • 34. The "tooth and nail" type of autosomal dominant ectodermal dysplasia.
    Giansanti JS, Long SM, Rankin JL.
    Oral Surg Oral Med Oral Pathol; 1974 Apr 04; 37(4):576-82. PubMed ID: 4521949
    [No Abstract] [Full Text] [Related]

  • 35. Frontofacionasal dysplasia: evidence for autosomal recessive inheritance.
    Gollop TR, Kiota MM, Martins RM, Lucchesi EA, Alvarenga Filho E.
    Am J Med Genet; 1984 Oct 04; 19(2):301-5. PubMed ID: 6439039
    [Abstract] [Full Text] [Related]

  • 36. New autosomal recessive form of amelia.
    Michaud J, Filiatrault D, Dallaire L, Lambert M.
    Am J Med Genet; 1995 Mar 27; 56(2):164-7. PubMed ID: 7625439
    [Abstract] [Full Text] [Related]

  • 37. Hypohidrotic ectodermal dysplasia (HED).
    Ahmed B, Yazdanie N.
    J Coll Physicians Surg Pak; 2006 Jan 27; 16(1):61-3. PubMed ID: 16441993
    [Abstract] [Full Text] [Related]

  • 38. Oculotrichodysplasia (OTD): a new probably autosomal recessive condition.
    Cecatto-De-Lima L, Pinheiro M, Freire-Maia N.
    J Med Genet; 1988 Jun 27; 25(6):430-2. PubMed ID: 3398012
    [Abstract] [Full Text] [Related]

  • 39. [A patient with anhidrotic ectodermal dysplasia].
    Wolff AA, Hermans JB.
    Ned Tijdschr Geneeskd; 1981 Dec 05; 125(49):2015-8. PubMed ID: 7322221
    [No Abstract] [Full Text] [Related]

  • 40. New cases of dermoodontodysplasia?
    Pinheiro M, Gomes-de-Sá-Filho FP, Freire-Maia N.
    Am J Med Genet; 1990 Jun 05; 36(2):161-6. PubMed ID: 2368802
    [Abstract] [Full Text] [Related]

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