These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

232 related items for PubMed ID: 6837633

  • 21. Christ-Siemens-Touraine syndrome--a clinical and genetic analysis of a large Brazilian kindred: II. Affected males.
    Pinheiro M, Freire-Maia N.
    Am J Med Genet; 1979; 4(2):123-8. PubMed ID: 574718
    [Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23. Brief clinical report: Curry-Hall syndrome.
    Shapiro SD, Jorgenson RJ, Salinas CF.
    Am J Med Genet; 1984 Mar; 17(3):579-83. PubMed ID: 6711608
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. 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; 29(5):486-8. PubMed ID: 15347331
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. [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
    [Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. Athelia in a female infant - heterozygous for anhidrotic ectodermal dysplasia.
    Burck U, Held KR.
    Clin Genet; 1981 Feb; 19(2):117-21. PubMed ID: 7471507
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Trichodermodysplasia with dental alterations: an apparently new genetic ectodermal dysplasia of the tricho-odonto-onychial subgroup.
    Pinheiro M, Freire-Maia DV, Miranda E, Silva-Filho OG, Freire-Maia N.
    Clin Genet; 1986 Apr; 29(4):332-6. PubMed ID: 3720011
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. Autosomal dominant onychodystrophy and congenital sensorineural deafness.
    Kondoh T, Tsuru A, Matsumoto T, Matsuzaka T, Tsuji Y.
    J Hum Genet; 1999 Apr; 44(1):60-2. PubMed ID: 9929981
    [Abstract] [Full Text] [Related]

  • 35. [Hidrotic ectodermal dysplasia].
    Altmeyer P, Schindera I.
    Hautarzt; 1975 Dec; 26(12):631-7. PubMed ID: 1213883
    [Abstract] [Full Text] [Related]

  • 36. The characterization of hereditary abnormalities of keratin: Clouston's ectodermal dysplasia.
    Reynold JM, Gold MB, Scriver CR.
    Birth Defects Orig Artic Ser; 1971 Jun; 7(8):91-5. PubMed ID: 5173317
    [Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. Ectodermal dysplasia with alopecia, onychodysplasia, hypohidrosis, keratoderma, abnormal teeth and deafness.
    Akhyani M, Kiavash K.
    Indian J Dermatol Venereol Leprol; 2007 Jun; 73(6):409-11. PubMed ID: 18032861
    [Abstract] [Full Text] [Related]

  • 40. An autosomal recessive ectodermal dysplasia syndrome of hypotrichosis, onychodysplasia, hyperkeratosis, kyphoscoliosis, catartact, and other manifestations.
    Alves AF, dos Santos PA, Castelo-Branco-Neto E, Freire-Maia N.
    Am J Med Genet; 1981 Jun; 10(3):213-8. PubMed ID: 7304669
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 12.