BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 3955862)

  • 1. A simple technique for recording and counting sweat pores on the dermal ridges.
    O'Leary E; Slaney J; Bryant DG; Fraser FC
    Clin Genet; 1986 Feb; 29(2):122-8. PubMed ID: 3955862
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal recessive anhidrotic ectodermal dysplasia: report of a case and discrimination of diagnostic features.
    Anton-Lamprecht I; Schleiermacher E; Wolf M
    Birth Defects Orig Artic Ser; 1988; 24(2):183-95. PubMed ID: 3179426
    [No Abstract]   [Full Text] [Related]  

  • 3. Induction of sweat glands by epidermal growth factor in murine X-linked anhidrotic ectodermal dysplasia.
    Blecher SR; Kapalanga J; Lalonde D
    Nature; 1990 Jun; 345(6275):542-4. PubMed ID: 2348861
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of functioning sweat pores and visualization of skin temperature patterns in X-linked hypohidrotic ectodermal dysplasia by whole body thermography.
    Clark RP; Goff MR; MacDermot KD
    Hum Genet; 1990 Nov; 86(1):7-13. PubMed ID: 2253940
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hypodontia and sweat pore counts in detecting carriers of X-linked hypohidrotic ectodermal dysplasia.
    Sofaer JA
    Br Dent J; 1981 Nov; 151(10):327-30. PubMed ID: 6946797
    [No Abstract]   [Full Text] [Related]  

  • 6. Autosomal recessive hypohidrotic ectodermal dysplasia with subclinical manifestation in the heterozygote.
    Passarge E; Fries E
    Birth Defects Orig Artic Ser; 1977; 13(3C):95-100. PubMed ID: 890117
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Manifestation of the lines of Blaschko in women heterozygous for X-linked hypohidrotic ectodermal dysplasia.
    Happle R; Frosch PJ
    Clin Genet; 1985 May; 27(5):468-71. PubMed ID: 4006271
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dermatoglyphics findings in families with X-linked hypohidrotic(or anhidrotic) ectodermal dysplasia(HED).
    Rodewald A; Zahn-Messow K
    Prog Clin Biol Res; 1982; 84():451-8. PubMed ID: 6896579
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypohidrotic ectodermal dysplasia: a genealogic, stereomicroscope, and scanning electron microscope study.
    Norval EJ; van Wyk CW; Basson NJ; Coldrey J
    Pediatr Dermatol; 1988 Aug; 5(3):159-66. PubMed ID: 3205855
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial simple hypohidrosis with abnormal palmar dermal ridges.
    Frydman M; Cohen HA; Kauschansky A; Matoth Y
    Am J Med Genet; 1988 Nov; 31(3):591-6. PubMed ID: 3228139
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Diminished sweat pores in hypohidrotic ectodermal dysplasia: a new method for assessment.
    Frias JL; Smith DW
    J Pediatr; 1968 May; 72(5):606-10. PubMed ID: 5646360
    [No Abstract]   [Full Text] [Related]  

  • 12. [A typical cases of X-linked anhidrotic ectodermal dysplasia and a diagnosis of carriers].
    Yamamoto Y; Fugisawa S; Morishima T; Morioka S; Iinuma K
    Nihon Hifuka Gakkai Zasshi; 1990 Mar; 100(4):527-32. PubMed ID: 2370706
    [TBL] [Abstract][Full Text] [Related]  

  • 13. X-linked recessive hypohidrotic ectodermal dysplasia. Manifestations and management.
    Wright JT; Finley WH
    Ala J Med Sci; 1986 Jan; 23(1):84-7. PubMed ID: 3953980
    [No Abstract]   [Full Text] [Related]  

  • 14. Hypohidrotic (anhidrotic) ectodermal dysplasia in female twins.
    Ogunrinde GO; Zubair RO; Ajike SO; Ige SO
    Niger J Clin Pract; 2012; 15(1):98-100. PubMed ID: 22437101
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Anhidrotic ectodermal dysplasia. Clinico-genetic study of 4 families].
    Balestrazzi P; Solli R; Salami P; Corrini L; Mattioli M; Bernasconi S
    Minerva Pediatr; 1979 Feb; 31(4):265-74. PubMed ID: 460084
    [No Abstract]   [Full Text] [Related]  

  • 16. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hypodontia, ectodermal dysplasia and sweat pore count.
    Tso MS; Crawford PJ; Miller J
    Br Dent J; 1985 Jan; 158(2):56-60. PubMed ID: 3855640
    [No Abstract]   [Full Text] [Related]  

  • 18. A novel missense mutation (402C-->T) in exon 1 in the EDA gene in a family with X-linked hypohidrotic ectodermal dysplasia.
    Hertz JM; Nørgaard Hansen K; Juncker I; Kjeldsen M; Gregersen N
    Clin Genet; 1998 Mar; 53(3):205-9. PubMed ID: 9630076
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia.
    Crawford PJ; Aldred MJ; Clarke A
    J Med Genet; 1991 Mar; 28(3):181-5. PubMed ID: 2051453
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autosomal dominant ectodermal dysplasia.
    Jorgenson RJ; Dowben JS; Dowben SL
    J Craniofac Genet Dev Biol; 1987; 7(4):403-12. PubMed ID: 3429615
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.