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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 7304669)

  • 1. 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; 10(3):213-8. PubMed ID: 7304669
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Possible second case of tricho-oculo-dermo-vertebral (Alves) syndrome.
    Stratton RF; Jorgenson RJ; Krause IC
    Am J Med Genet; 1993 May; 46(3):313-5. PubMed ID: 8488878
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An ectodermal dysplasia syndrome of alopecia, onychodysplasia, hypohidrosis, hyperkeratosis, deafness and other manifestations.
    Freire-Maia N; Cat I; Raponegaidzinski R
    Hum Hered; 1977; 27(2):127-33. PubMed ID: 863459
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Autosomal recessive ectodermal dysplasia--a special nosologic entity? (author's transl)].
    Lelis J
    Dermatol Monatsschr; 1979 Aug; 165(8):587-92. PubMed ID: 159839
    [No Abstract]   [Full Text] [Related]  

  • 6. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pilodentoungulardysplasia with microcephaly: a new ectodermal dysplasia/malformation syndrome.
    Tajara EH; Pinheiro M; Freire-Maia N
    Am J Med Genet; 1987 Jan; 26(1):153-6. PubMed ID: 3812555
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pili torti and onychodysplasia. Report of a previously undescribed hidrotic ectodermal dysplasia.
    Calzavara-Pinton P; Carlino A; Benetti A; De Panfilis G
    Dermatologica; 1991; 182(3):184-7. PubMed ID: 1879585
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 12. Cataracts, alopecia, and sclerodactyly: a previously apparently undescribed ectodermal dysplasia syndrome on the island of Rodrigues.
    Wallis C; Ip FS; Beighton P
    Am J Med Genet; 1989 Apr; 32(4):500-3. PubMed ID: 2773993
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her child.
    Moerman P; Fryns JP
    Am J Med Genet; 1996 Jun; 63(3):479-81. PubMed ID: 8737656
    [TBL] [Abstract][Full Text] [Related]  

  • 14. ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia.
    Propping P; Zerres K
    Am J Med Genet; 1993 Mar; 45(5):642-8. PubMed ID: 8456838
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome).
    Steiner CE; Cintra ML; Marques-de-Faria AP
    Am J Med Genet; 2002 Dec; 113(4):381-4. PubMed ID: 12457412
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Anodontia and hidrotic ectodermal dysplasia, hyporeactive to heat. Effect of acitretin].
    Mashshini-Jason F; Wolff P; Piérard GE; Lapière CM
    Ann Dermatol Venereol; 1994; 121(2):120-2. PubMed ID: 7979018
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A distinct type of hidrotic ectodermal dysplasia.
    Halal F; Setton N; Wang NS
    Am J Med Genet; 1991 Mar; 38(4):552-6. PubMed ID: 2063897
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signs.
    Freire-Maia N; Fortes VA; Pereira LC; Opitz JM; Marcalle FA; Cavalli IJ
    J Med Genet; 1975 Sep; 12(3):308-10. PubMed ID: 1177286
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental retardation.
    Ohdo S; Madokoro H; Sonoda T; Takei M; Yasuda H; Mori N
    J Med Genet; 1987 Oct; 24(10):609-12. PubMed ID: 3681906
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.