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 *

92 related articles for article (PubMed ID: 2989220)

  • 1. [Hereditary sclerodactyly and syndactyly].
    Eubel R; Klose L; Mahrle G
    Hautarzt; 1985 May; 36(5):302-4. PubMed ID: 2989220
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The CRST syndrome (calcinosis, Raynaud's phenomenon, sclerodactyly and telangiectasia).
    Brown AE
    Br J Oral Surg; 1976 Nov; 14(2):137-42. PubMed ID: 1070339
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Sclero-atrophic keratodermal genodermatosis of the extremities (sclerotylosis) (author's transl)].
    Lambert D; Nivelon-Chevallier A; Chapuis JL
    J Genet Hum; 1978 Mar; 26(1):25-31. PubMed ID: 670936
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The scleroatrophic syndrome of Huriez: a cancer-prone genodermatosis.
    Hamm H; Traupe H; Bröcker EB; Schubert H; Kolde G
    Br J Dermatol; 1996 Mar; 134(3):512-8. PubMed ID: 8731679
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Calcinosis-Raynaud's disease-sclerodactylia-telangiectasis syndrome].
    Texier L; Sarrat L; Géniaux M; Gauthier O; Tamisier JM
    Bull Soc Fr Dermatol Syphiligr; 1971; 78(1):53-4. PubMed ID: 5565930
    [No Abstract]   [Full Text] [Related]  

  • 6. Dominant inheritance of syn-camptodactyly of the second and third toes with foot and lower limb asymmetry and scoliosis.
    Halal F
    Am J Med Genet; 1985 Sep; 22(1):149-56. PubMed ID: 4050850
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Genetic analysis of a Chinese pedigree with congenital synpolydactyly].
    Qin W; Shu AL; Xing QH; Yang MS; Feng GY; He L
    Yi Chuan Xue Bao; 2003 Oct; 30(10):973-7. PubMed ID: 14669516
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?
    Majewski E; Goecke T; Meinecke P
    Am J Med Genet; 1996 May; 63(1):185-9. PubMed ID: 8723107
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Papular mucinosis associated with scleroderma.
    Sawada Y; Seishima M; Funabashi M; Noda T; Maeda M; Kitajima Y
    Eur J Dermatol; 1998; 8(7):497-500. PubMed ID: 9854162
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Syndactyly type V.
    Robinow M; Johnson GF; Broock GJ
    Am J Med Genet; 1982 Apr; 11(4):475-82. PubMed ID: 6283889
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Synpolydactyly: unusual features and variable expression in 5 generations of an Italian family].
    Chessa Ricotti G; Lapi E; De Bernardi A; Corti P
    Pediatr Med Chir; 1990; 12(3):259-63. PubMed ID: 2177188
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Poly-syndactyly of hands and feet with talipes equino-varus. An unusual combination.
    Gadegone WM; Kumar K
    J Hand Surg Br; 1984 Jun; 9(2):149-50. PubMed ID: 6086792
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dry hands in scleroderma. Including studies of sweat gland function in healthy individuals.
    Serup J; Rasmussen I
    Acta Derm Venereol; 1985; 65(5):419-23. PubMed ID: 2416166
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A case of progressive systemic sclerosis accompanied with rheumatoid arthritis].
    Shimomura C; Eguchi K; Mine M; Tezuka H; Matsunaga M; Ueki Y; Otsubo T; Nakao H; Migita K; Kawakami A
    Ryumachi; 1989 Aug; 29(4):284-90. PubMed ID: 2617370
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal dominant inheritance of hypothalamic hamartoma associated with polysyndactyly: heterogeneity or variable expressivity?
    Grebe TA; Clericuzio C
    Am J Med Genet; 1996 Dec; 66(2):129-37. PubMed ID: 8958318
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial microtia in four generations with variable expressivity and incomplete penetrance in association with type I syndactyly.
    Balci S; Boduroğlu K; Kaya S
    Turk J Pediatr; 2001; 43(4):362-5. PubMed ID: 11765172
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A pedigree of cervical stenosis, brachydactyly, syndactyly, and hyperopia.
    Iida H; Shikata J; Yamamuro T; Takeda N; Ueba Y
    Clin Orthop Relat Res; 1989 Oct; (247):80-6. PubMed ID: 2551554
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Desyndactylization: a unique case report.
    Dowdy NL; Puleo DC
    J Foot Surg; 1991; 30(4):340-3. PubMed ID: 1658110
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Unilateral limited scleroderma-like changes following formation of an arteriovenous fistula.
    Roberts H; Curnow PA
    Australas J Dermatol; 2007 Feb; 48(1):37-9. PubMed ID: 17222301
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pseudoainhum associated with linear scleroderma.
    Park BS; Hyun Cho K; Youn JI; Chung JH
    Arch Dermatol; 1996 Dec; 132(12):1520-1. PubMed ID: 8961892
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.